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Below is a list of high-confidence human gene-fly ortholog pairs for which there is also high-confidence evidence that the human gene is implicated in disease. The disease gene relationships are from the NCBI Online Mendelian Inheritance in Man database. The ortholog relationships are based on DIOPT scores (scores of 8, 9 or 10; see Hu et al. 2011 BMC Bioinformatics and flyrnai.org/DIOPT). Please note that you can find more putative fly ortholog genes (DIOPT scores of 1 or more) searching with the same disease term at DIOPT-DIST. This is meant as a high-confidence starting off point. It is not a comprehensive list of fly gene-human disease gene relationships.

We have made note below of what VALIUM20 construct RNAi fly stocks are available. All of these genes have been nominated for TRiP VALIUM20 fly stock production so more lines should be available for these genes in the future. Please note that this is not a comprehensive list of all TRiP or all fly RNAi lines available, as other TRiP stocks (e.g. VALIUM22) and other collections (e.g. NIG-Japan and VDRC) are also available for some of these genes. You can use UP-TORR to search all three collections.

We gratefully acknowledge support from ORIP/NCRR R24 RR032668 to N. Perrimon.

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The data on this page was last updated Feb 27, 2015

Download List (in .xlsx format)

Human disease gene Human gene description Entrez Human GeneID OMIM ID Disease Category
(for disease names click DIOPT score)
DIOPT score Fly gene symbol Fly gene name FlyBase GeneID CG BDSC Stock IDs RSVP Data
AARS alanyl-tRNA synthetase 16 601065 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Aats-ala Alanyl-tRNA synthetase FBgn0027094 CG13391
ABAT 4-aminobutyrate aminotransferase 18 137150 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG7433 - FBgn0036927 CG7433 54993 HMC03730
ABCA3 ATP-binding cassette, sub-family A (ABC1), member 3 21 601615 Musculoskeletal Diseases, Respiratory Tract Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG1718 - FBgn0031170 CG1718 38329, 38353 HMS01796, HMS01821
ABCB7 ATP-binding cassette, sub-family B (MDR/TAP), member 7 22 300135 Nervous System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 ABCB7 - FBgn0035244 CG7955 51696 HMC03142
ACACA acetyl-CoA carboxylase alpha 31 200350 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 ACC Acetyl-CoA carboxylase FBgn0033246 CG11198 34885 HMS01230
ACADM acyl-CoA dehydrogenase, C-4 to C-12 straight chain 34 607008 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CG12262 - FBgn0035811 CG12262 32436, 32437 HMS00435, HMS00434
ACADS acyl-CoA dehydrogenase, C-2 to C-3 short chain 35 606885 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 10 Arc42 Arc42 FBgn0038742 CG4703 53287 HMC03503
ACADSB acyl-CoA dehydrogenase, short/branched chain 36 600301 Musculoskeletal Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CG3902 - FBgn0036824 CG3902 HMC04101
ACADVL acyl-CoA dehydrogenase, very long chain 37 609575 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 8 CG7461 - FBgn0034432 CG7461 HMC04034
ACAT1 acetyl-CoA acetyltransferase 1 38 607809 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases 10 CG10932 - FBgn0029969 CG10932 51785 HMC03340
ACAT2 acetyl-CoA acetyltransferase 2 39 100678 Musculoskeletal Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 10 CG9149 - FBgn0035203 CG9149
ACOX1 acyl-CoA oxidase 1, palmitoyl 51 609751 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 8 CG5009 - FBgn0027572 CG5009 52882 HMC03620
ACTN2 actinin, alpha 2 88 102573 Cardiovascular Diseases 9 Actn alpha actinin FBgn0000667 CG4376 34874 HMS00193
ACVR1 activin A receptor, type I 90 102576 Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 sax saxophone FBgn0003317 CG1891 42546, 57319 HMJ02118, HMC04135, HMS04520
ADD1 adducin 1 (alpha) 118 102680 Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 hts hu li tai shao FBgn0263391 CG43443 38283 HMS01736
ADK adenosine kinase 132 102750 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 AdenoK Adenosine Kinase FBgn0036337 CG11255
AGA aspartylglucosaminidase 175 613228 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 CG1827 - FBgn0033431 CG1827
AGA aspartylglucosaminidase 175 613228 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 9 CG10474 - FBgn0034427 CG10474 51444 HMC03158
AGL amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase 178 610860 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 CG9485 - FBgn0034618 CG9485 34333 HMS01321, HMJ22420
JAG1 jagged 1 182 601920 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms 8 Ser Serrate FBgn0004197 CG6127 34700 HMS01179
AGXT alanine-glyoxylate aminotransferase 189 604285 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 Spat Serine pyruvate aminotransferase FBgn0014031 CG3926 51935 HMC03220
AHCY adenosylhomocysteinase 191 180960 Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 Ahcy13 Adenosylhomocysteinase at 13 FBgn0014455 CG11654 51477 HMC03222
AK1 adenylate kinase 1 203 103000 Hemic and Lymphatic Diseases 10 Adk1 Adenylate kinase-1 FBgn0022709 CG17146 51799 HMC03355
AK2 adenylate kinase 2 204 103020 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Immune System Diseases 10 Adk2 Adenylate kinase-2 FBgn0022708 CG3140 HMC04007
ALAS2 aminolevulinate, delta-, synthase 2 212 301300 Digestive System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 Alas Aminolevulinate synthase FBgn0020764 CG3017 54815, 51489 HMC03240, HMJ21534
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial) 217 100650 Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 Aldh Aldehyde dehydrogenase FBgn0012036 CG3752 34989 HMS01399
ALDH3A2 aldehyde dehydrogenase 3 family, member A2 224 609523 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 8 Aldh-III Aldehyde dehydrogenase type III FBgn0010548 CG11140 51820 HMC03391
ALDOA aldolase A, fructose-bisphosphate 226 103850 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases, Immune System Diseases 10 Ald Aldolase FBgn0000064 CG6058
AMT aminomethyltransferase 275 238310 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 10 CG6415 - FBgn0032287 CG6415 51867 HMC03441
SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4 291 103220 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, Mental Disorders 9 sesB stress-sensitive B FBgn0003360 CG16944 36661 HMS01549
APP amyloid beta (A4) precursor protein 351 104760 Nervous System Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 7 Appl beta amyloid protein precursor-like FBgn0000108 CG7727 39013 HMS01931
APRT adenine phosphoribosyltransferase 353 102600 Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications 10 Aprt Adenine phosphoribosyltransferase FBgn0000109 CG18315
ARG1 arginase, liver 383 608313 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 arg arginase FBgn0023535 CG18104 HMC04102
ARNT aryl hydrocarbon receptor nuclear translocator 405 126110 Neoplasms 8 tgo tango FBgn0264075 CG11987 53351 HMC03580
ASS1 argininosuccinate synthase 1 445 603470 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG1315 - FBgn0026565 CG1315 53323 HMC03552
ATIC 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase 471 601731 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG11089 - FBgn0039241 CG11089 53332, 58121 HMC03561, HMJ22058
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide 478 182350 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 8 Atpalpha Na pump alpha subunit FBgn0002921 CG5670 32913, 33646 HMS00703, HMS00047
ATP2A1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 487 108730 Musculoskeletal Diseases 10 Ca-P60A Calcium ATPase at 60A FBgn0263006 CG3725 44581 HMS02878
ALDH7A1 aldehyde dehydrogenase 7 family, member A1 501 107323 Respiratory Tract Diseases, Nervous System Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG9629 - FBgn0036857 CG9629
KIF1A kinesin family member 1A 547 601255 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Pathological Conditions, Signs and Symptoms 9 unc-104 unc-104 ortholog (C. elegans) FBgn0267002 CG8566 53296, 58083 HMC03512, HMJ21975
AUH AU RNA binding protein/enoyl-CoA hydratase 549 600529 Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CG8778 - FBgn0033761 CG8778
BBS4 Bardet-Biedl syndrome 4 585 600374 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 BBS4 Bardet-Biedl syndrome 4 ortholog (H. sapiens) FBgn0033578 CG13232 53305 HMC03532
BCAT1 branched chain amino-acid transaminase 1, cytosolic 586 113520 Disease risk factor, diagnosis or treatment 9 CG1673 - FBgn0030482 CG1673 38363 HMS01832
BCS1L BCS1-like (S. cerevisiae) 617 603647 Musculoskeletal Diseases, Digestive System Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 10 CG4908 - FBgn0032195 CG4908 51863 HMC03437
BLMH bleomycin hydrolase 642 602403 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 10 CG1440 - FBgn0030038 CG1440 44521 HMC02912
BRAF v-raf murine sarcoma viral oncogene homolog B1 673 164757 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 phl pole hole FBgn0003079 CG2845 HMC04133, HMC03854
BTD biotinidase 686 609019 Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Immune System Diseases 6 vanin-like vanin-like FBgn0040069 CG32754
BTD biotinidase 686 609019 Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Immune System Diseases 6 CG32751 - FBgn0052751 CG32751 50653 HMC03054
SLC25A20 solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 788 613698 Musculoskeletal Diseases, Digestive System Diseases, Nervous System Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 colt congested-like trachea FBgn0019830 CG3057 51798 HMC03354
CAT catalase 847 115500 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 Cat Catalase FBgn0000261 CG6871 34020 HMS00990
CBFB core-binding factor, beta subunit 865 121360 Neoplasms, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Bgb Big brother FBgn0013753 CG7959
CBS cystathionine-beta-synthase 875 613381 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Cbs Cystathionine beta-synthase FBgn0031148 CG1753 36767 HMS03028
CDC6 cell division cycle 6 homolog (S. cerevisiae) 990 602627 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms 9 Cdc6 Cdc6 FBgn0035918 CG5971 HMC03802
CHAT choline O-acetyltransferase 1103 118490 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Immune System Diseases 9 Cha Choline acetyltransferase FBgn0000303 CG12345
CHM choroideremia (Rab escort protein 1) 1121 300390 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Rep Rab escort protein FBgn0026378 CG8432 51851 HMC03425
CHN1 chimerin (chimaerin) 1 1123 118423 Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 RhoGAP5A Rho GTPase activating protein at 5A FBgn0029778 CG3208 HMJ02220
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal) 1139 118511 Mental Disorders 8 nAChRalpha6 nicotinic Acetylcholine Receptor alpha6 FBgn0032151 CG4128 52885 HMC03623
CLCN2 chloride channel, voltage-sensitive 2 1181 600570 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 ClC-a Chloride channel-a FBgn0051116 CG31116 53337 HMC03566
CLCN7 chloride channel, voltage-sensitive 7 1186 602727 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 ClC-b Chloride channel-b FBgn0033755 CG8594 51877 HMC03451
CLN3 ceroid-lipofuscinosis, neuronal 3 1201 607042 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 cln3 cln3 FBgn0036756 CG5582 35734 HMS01476
COMP cartilage oligomeric matrix protein 1311 600310 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Tsp Thrombospondin FBgn0031850 CG11326 34661, 44116 HMS01138, HMS02838
COX6B1 cytochrome c oxidase subunit VIb polypeptide 1 (ubiquitous) 1340 124089 Musculoskeletal Diseases, Digestive System Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 COX6B Cytochrome c oxidase subunit 6B FBgn0031066 CG14235
COX10 COX10 homolog, cytochrome c oxidase assembly protein, heme A: farnesyltransferase (yeast) 1352 602125 Nervous System Diseases 9 CG5037 - FBgn0032222 CG5037 51864 HMC03438
COX15 COX15 homolog, cytochrome c oxidase assembly protein (yeast) 1355 603646 Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 9 CG3803 - FBgn0034938 CG3803 42948, 35731 HMS01473, HMS02641
CPOX coproporphyrinogen oxidase 1371 612732 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases, Mental Disorders 10 Coprox Coproporphyrinogen oxidase FBgn0021944 CG3433 HMC04005
CPT1A carnitine palmitoyltransferase 1A (liver) 1374 600528 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 whd withered FBgn0261862 CG12891 34066, 33635 HMS00040, HMS00033
CPT2 carnitine palmitoyltransferase 2 1376 600650 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Immune System Diseases, Mental Disorders 10 CG2107 - FBgn0035383 CG2107 51900 HMC03474
CRAT carnitine O-acetyltransferase 1384 600184 Nutritional and Metabolic Diseases 9 CRAT Carnitine O-Acetyl-Transferase FBgn0037440 CG1041 52921 HMC03661
CRYAB crystallin, alpha B 1410 123590 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases 9 l(2)efl lethal (2) essential for life FBgn0011296 CG4533 51816, 41724 HMC03387, HMS02290
CRYM crystallin, mu 1428 123740 Otorhinolaryngologic Diseases, Nervous System Diseases, Pathological Conditions, Signs and Symptoms 10 CG4872 - FBgn0030799 CG4872
CTH cystathionase (cystathionine gamma-lyase) 1491 607657 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease risk factor, diagnosis or treatment 10 Eip55E Eip55E FBgn0000566 CG5345 36766 HMS03027
CTNS cystinosin, lysosomal cystine transporter 1497 606272 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Endocrine System Diseases, Immune System Diseases 9 CG17119 - FBgn0039045 CG17119 40823 HMS00213
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa 1499 116806 Neoplasms, Digestive System Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 arm armadillo FBgn0000117 CG11579 35004 HMS01414
CTSD cathepsin D 1509 116840 Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 8 cathD cathD FBgn0029093 CG1548 53882 HMC03859, HMJ21197
CYLD cylindromatosis (turban tumor syndrome) 1540 605018 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 CYLD cylindromatosis ortholog (H. sapiens) FBgn0032210 CG5603 40840 HMS02006
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase) 1621 609312 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Disease risk factor, diagnosis or treatment 10 Tbh Tyramine beta hydroxylase FBgn0010329 CG1543 HMC03358
DBT dihydrolipoamide branched chain transacylase E2 1629 248610 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CG5599 - FBgn0030612 CG5599 32876 HMS00663
DCTN1 dynactin 1 1639 601143 Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 9 Gl Glued FBgn0001108 CG9206
DDB1 damage-specific DNA binding protein 1, 127kDa 1642 600045 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 pic piccolo FBgn0260962 CG7769 33888, 41997 HMS00826, HMS02398
DDC dopa decarboxylase (aromatic L-amino acid decarboxylase) 1644 107930 Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Mental Disorders 10 Ddc Dopa decarboxylase FBgn0000422 CG10697 51462 HMC03200
DDX11 DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11 1663 601150 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 CG11403 - FBgn0026876 CG11403 50991, 51800 HMJ21102, HMC03357, HMJ21701
DHODH dihydroorotate dehydrogenase (quinone) 1723 126064 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Dhod Dihydroorotate dehydrogenase FBgn0000447 CG9741 51801 HMC03359
DIAPH2 diaphanous homolog 2 (Drosophila) 1730 300108 Female Urogenital Diseases and Pregnancy Complications, Endocrine System Diseases 7 dia diaphanous FBgn0011202 CG1768 33424 HMS00308
DKC1 dyskeratosis congenita 1, dyskerin 1736 300126 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 Nop60B Nucleolar protein at 60B FBgn0259937 CG3333 57500 HMC04815
DLAT dihydrolipoamide S-acetyltransferase 1737 608770 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CG5261 - FBgn0031912 CG5261 40922 HMS02170
DLD dihydrolipoamide dehydrogenase 1738 238331 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 8 CG7430 - FBgn0036762 CG7430
DMD dystrophin 1756 300377 Musculoskeletal Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 Dys Dystrophin FBgn0260003 CG34157 HMC03789
SARDH sarcosine dehydrogenase 1757 604455 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 Sardh Sarcosine dehydrogenase FBgn0034276 CG6385 51883 HMC03457
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1 1778 600112 Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Pathological Conditions, Signs and Symptoms 9 Dhc64C Dynein heavy chain 64C FBgn0261797 CG7507 36698 HMS01587
DPAGT1 dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase) 1798 191350 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 CG5287 - FBgn0032477 CG5287 51869 HMC03443
DPYD dihydropyrimidine dehydrogenase 1806 612779 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 10 su(r) suppressor of rudimentary FBgn0086450 CG2194 53339 HMC03568
DPYS dihydropyrimidinase 1807 613326 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CRMP Collapsin Response Mediator Protein FBgn0023023 CG1411 53354 HMC03583
TOR1A torsin family 1, member A (torsin A) 1861 605204 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms, Mental Disorders 9 Torsin Torsin FBgn0025615 CG3024 50620 HMC02987
ECE1 endothelin converting enzyme 1 1889 600423 Digestive System Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Nep3 Neprilysin 3 FBgn0031081 CG9565 50930 HMJ21024
EIF2B1 eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa 1967 606686 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, Mental Disorders 10 eIF2B-alpha eIF2B-alpha FBgn0039726 CG7883 HMC03768
EIF4G1 eukaryotic translation initiation factor 4 gamma, 1 1981 600495 Nervous System Diseases 8 eIF4G eukaryotic translation initiation factor 4G FBgn0023213 CG10811 33049 HMS00762
ELAVL4 ELAV (embryonic lethal, abnormal vision, Drosophila)-like 4 1996 168360 Nervous System Diseases 9 fne found in neurons FBgn0086675 CG4396 53340 HMC03569
ENO1 enolase 1, (alpha) 2023 172430 Nutritional and Metabolic Diseases 9 Eno Enolase FBgn0000579 CG17654
EP300 E1A binding protein p300 2033 602700 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases, Mental Disorders 10 nej nejire FBgn0261617 CG15319 37489, 36682 HMS01570, HMS01507
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic) 2052 132810 Musculoskeletal Diseases, Digestive System Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Jheh1 Juvenile hormone epoxide hydrolase 1 FBgn0010053 CG15101 50676 HMC03077
ERCC1 excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence) 2067 126380 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases 9 Ercc1 Ercc1 FBgn0028434 CG10215 52929 HMC03670
ERCC2 excision repair cross-complementing rodent repair deficiency, complementation group 2 2068 126340 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 Xpd Xeroderma pigmentosum D ortholog (H. sapiens) FBgn0261850 CG9433 53992 HMJ21396
ERCC3 excision repair cross-complementing rodent repair deficiency, complementation group 3 2071 133510 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases, Immune System Diseases 8 hay haywire FBgn0001179 CG8019 53345 HMC03574
ERCC4 excision repair cross-complementing rodent repair deficiency, complementation group 4 2072 133520 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Immune System Diseases 9 mei-9 meiotic 9 FBgn0002707 CG3697 HMC04000, HMJ22204
ESRRB estrogen-related receptor beta 2103 602167 Otorhinolaryngologic Diseases, Nervous System Diseases, Pathological Conditions, Signs and Symptoms 9 ERR estrogen-related receptor FBgn0035849 CG7404 50686 HMC03087
ETFA electron-transfer-flavoprotein, alpha polypeptide 2108 608053 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 wal walrus FBgn0010516 CG8996 34915 HMS01263
G6PD glucose-6-phosphate dehydrogenase 2539 305900 Digestive System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 Zw Zwischenferment FBgn0004057 CG12529 50667 HMC03068
GAD1 glutamate decarboxylase 1 (brain, 67kDa) 2571 605363 Musculoskeletal Diseases, Nervous System Diseases 9 Gad1 Glutamic acid decarboxylase 1 FBgn0004516 CG14994 51794 HMC03350
GALE UDP-galactose-4-epimerase 2582 606953 Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 Gale UDP-galactose 4'-epimerase FBgn0035147 CG12030 44496 HMC02429
GALT galactose-1-phosphate uridylyltransferase 2592 606999 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Galt Galactose-1-phosphate uridylyltransferase FBgn0263200 CG9232 HMC03885
GARS glycyl-tRNA synthetase 2617 600287 Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Aats-gly Glycyl-tRNA synthetase FBgn0027088 CG6778 HMC04014
GBA glucosidase, beta, acid 2629 606463 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases, Mental Disorders 8 CG31148 - FBgn0051148 CG31148 39064, 38379 HMS01984, HMS01848
GBA glucosidase, beta, acid 2629 606463 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases, Mental Disorders 8 CG31414 - FBgn0051414 CG31414 38970, 38977 HMS01885, HMS01893
GBE1 glucan (1,4-alpha-), branching enzyme 1 2632 607839 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 AGBE 1,4-Alpha-Glucan Branching Enzyme FBgn0053138 CG33138 40860 HMS02027
GCDH glutaryl-CoA dehydrogenase 2639 608801 Musculoskeletal Diseases, Digestive System Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG9547 - FBgn0031824 CG9547 44556, 53327 HMC03556, HMS02852
GCH1 GTP cyclohydrolase 1 2643 600225 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Pathological Conditions, Signs and Symptoms, Mental Disorders 9 Pu Punch FBgn0003162 CG9441 41998 HMC04085, HMS02399
GCSH glycine cleavage system protein H (aminomethyl carrier) 2653 238330 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 10 ppl pumpless FBgn0027945 CG7758 51778, 52983 HMJ21670, HMC03333
GDI1 GDP dissociation inhibitor 1 2664 300104 Nervous System Diseases, Pathological Conditions, Signs and Symptoms 9 Gdi GDP dissociation inhibitor FBgn0004868 CG4422 57502 HMC04817
GFER growth factor, augmenter of liver regeneration 2671 600924 Musculoskeletal Diseases, Nervous System Diseases 9 Alr Augmenter of liver regeneration FBgn0031068 CG12534
GGCX gamma-glutamyl carboxylase 2677 137167 Musculoskeletal Diseases, Stomatognathic Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 GC gamma-glutamyl carboxylase FBgn0035245 CG13927 51897 HMC03471
GK glycerol kinase 2710 300474 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Endocrine System Diseases 10 Gyk Glycerol kinase FBgn0025592 CG18374 51849 HMC03423
GCLC glutamate-cysteine ligase, catalytic subunit 2729 606857 Musculoskeletal Diseases, Nervous System Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Pathological Conditions, Signs and Symptoms 10 Gclc Glutamate-cysteine ligase catalytic subunit FBgn0040319 CG2259
GCLM glutamate-cysteine ligase, modifier subunit 2730 601176 Cardiovascular Diseases, Pathological Conditions, Signs and Symptoms 10 Gclm Glutamate-cysteine ligase modifier subunit FBgn0046114 CG4919 58075 HMJ21967
GLE1 GLE1 RNA export mediator homolog (yeast) 2733 603371 Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 8 CG14749 - FBgn0033316 CG14749 52888 HMC03626
GLUD1 glutamate dehydrogenase 1 2746 138130 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 10 Gdh Glutamate dehydrogenase FBgn0001098 CG5320 51473 HMC03217
GLUL glutamate-ammonia ligase 2752 138290 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 Gs2 Glutamine synthetase 2 FBgn0001145 CG1743 40949 HMS02197
GNAQ guanine nucleotide binding protein (G protein), q polypeptide 2776 600998 Pathological Conditions, Signs and Symptoms 10 Galphaq G protein alpha q subunit FBgn0004435 CG17759 33765, 36775 JF02390, JF02464
GNRHR gonadotropin-releasing hormone receptor 2798 138850 Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 8 AkhR Adipokinetic hormone receptor FBgn0025595 CG11325 51710 HMC03228
SLC7A9 solute carrier family 7 (glycoprotein-associated amino acid transporter light chain, bo,+ system), member 9 11136 604144 Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG9413 - FBgn0030574 CG9413 51791 HMC03347
GLMN glomulin, FKBP associated protein 11146 601749 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG30496 - FBgn0050496 CG30496 44078 HMC04021, HMS02795
TREH trehalase (brush-border membrane glycoprotein) 11181 275360 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 Treh Trehalase FBgn0003748 CG9364 51810 HMC03381
CHEK2 checkpoint kinase 2 11200 604373 Neoplasms, Musculoskeletal Diseases, Male Urogenital Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Pathological Conditions, Signs and Symptoms 9 lok loki FBgn0019686 CG10895
AKAP10 A kinase (PRKA) anchor protein 10 11216 604694 Nervous System Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Trait 9 pkaap pkaap FBgn0040079 CG4132 HMC04020
SEC63 SEC63 homolog (S. cerevisiae) 11231 608648 Musculoskeletal Diseases, Digestive System Diseases, Respiratory Tract Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Sec63 Sec63 ortholog (S. cerevisiae) FBgn0035771 CG8583 52925 HMC03666
PDCD10 programmed cell death 10 11235 609118 Nervous System Diseases 10 Ccm3 Cerebral cavernous malformation 3 ortholog FBgn0038331 CG5073 53283 HMC03499
RNF139 ring finger protein 139 11236 603046 Neoplasms, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications 9 Trc8 TRC8 ortholog FBgn0039668 CG2304 HMC04111
PNKP polynucleotide kinase 3'-phosphatase 11284 605610 Musculoskeletal Diseases, Nervous System Diseases 10 CG9601 - FBgn0037578 CG9601 39003 HMS01919
B4GALT7 xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 (galactosyltransferase I) 11285 604327 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 beta4GalT7 beta-4-galactosyltransferase 7 FBgn0039258 CG11780
DOLK dolichol kinase 22845 610746 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 CG8311 - FBgn0034141 CG8311 52926 HMC03667
CHSY1 chondroitin sulfate synthase 1 22856 608183 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Pathological Conditions, Signs and Symptoms, Mental Disorders 10 CG9220 - FBgn0030662 CG9220 51787 HMC03343
RAB3GAP1 RAB3 GTPase activating protein subunit 1 (catalytic) 22930 602536 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 CG31935 - FBgn0051935 CG31935
CCT5 chaperonin containing TCP1, subunit 5 (epsilon) 22948 610150 Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Cct5 T-complex Chaperonin 5 FBgn0010621 CG8439 57440 HMC04747
RSPH9 radial spoke head 9 homolog (Chlamydomonas) 221421 612648 Respiratory Tract Diseases, Otorhinolaryngologic Diseases 10 CG31803 - FBgn0051803 CG31803 53338 HMC03567
MSRB3 methionine sulfoxide reductase B3 253827 613719 Otorhinolaryngologic Diseases, Nervous System Diseases, Pathological Conditions, Signs and Symptoms 9 SelR Selenoprotein R FBgn0267376 CG6584 52919 HMC03659
BRWD3 bromodomain and WD repeat domain containing 3 254065 300553 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Male Urogenital Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 BRWD3 BRWD3 FBgn0011785 CG31132 33421 HMS00304
MFSD8 major facilitator superfamily domain containing 8 256471 611124 Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG8596 - FBgn0035767 CG8596 HMC03819
SUMF1 sulfatase modifying factor 1 285362 607939 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 CG7049 - FBgn0035102 CG7049 51896 HMC03470
CYP4V2 cytochrome P450, family 4, subfamily V, polypeptide 2 285440 608614 Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Cyp4c3 Cytochrome P450-4c3 FBgn0015032 CG1438 HMC03873
CCDC39 coiled-coil domain containing 39 339829 613798 Respiratory Tract Diseases, Otorhinolaryngologic Diseases 9 CG17387 - FBgn0037276 CG17387 53273 HMC03489
RSPH4A radial spoke head 4 homolog A (Chlamydomonas) 345895 612647 Respiratory Tract Diseases, Otorhinolaryngologic Diseases 10 CG3121 - FBgn0034957 CG3121 38524 HMS01721
SLC26A5 solute carrier family 26, member 5 (prestin) 375611 604943 Otorhinolaryngologic Diseases, Nervous System Diseases, Pathological Conditions, Signs and Symptoms 7 Prestin Prestin FBgn0036770 CG5485 50706 HMC03108
D2HGDH D-2-hydroxyglutarate dehydrogenase 728294 609186 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 8 CG3835 - FBgn0023507 CG3835 53355 HMC03584
GNS glucosamine (N-acetyl)-6-sulfatase 2799 607664 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases, Mental Disorders 10 CG18278 - FBgn0033836 CG18278 51878 HMC03452
GPD1 glycerol-3-phosphate dehydrogenase 1 (soluble) 2819 138420 Musculoskeletal Diseases, Digestive System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 Gpdh Glycerol 3 phosphate dehydrogenase FBgn0001128 CG9042 51474 HMC03218
GPD2 glycerol-3-phosphate dehydrogenase 2 (mitochondrial) 2820 138430 Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 8 Gpo-1 Glycerophosphate oxidase-1 FBgn0022160 CG8256 HMC04006
GPI glucose-6-phosphate isomerase 2821 172400 Musculoskeletal Diseases, Digestive System Diseases, Nervous System Diseases, Hemic and Lymphatic Diseases, Skin and Connective Tissue Diseases 10 Pgi Phosphoglucose isomerase FBgn0003074 CG8251 51804 HMC03362
GSS glutathione synthetase 2937 601002 Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG32495 - FBgn0052495 CG32495 54017, 53910 HMJ21443, HMC03776, HMJ21241
GSTZ1 glutathione S-transferase zeta 1 2954 603758 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 GstZ1 Glutathione S transferase Z1 FBgn0037696 CG9362 53280 HMC03496
GSTZ1 glutathione S-transferase zeta 1 2954 603758 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 8 GstZ2 Glutathione S transferase Z2 FBgn0037697 CG9363 HMJ21334, HMC03781
MSH6 mutS homolog 6 (E. coli) 2956 600678 Neoplasms, Digestive System Diseases, Stomatognathic Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Msh6 Msh6 FBgn0036486 CG7003 35737 HMS01479
GUSB glucuronidase, beta 2990 611499 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 CG15117 - FBgn0034417 CG15117 33693 HMS00562
GYS1 glycogen synthase 1 (muscle) 2997 138570 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 GlyS Glycogen synthase FBgn0266064 CG6904 34930, 50956 HMS01279, HMJ21058
HSD17B10 hydroxysteroid (17-beta) dehydrogenase 10 3028 300256 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Pathological Conditions, Signs and Symptoms, Mental Disorders 10 scu scully FBgn0021765 CG7113 41884 HMS02305
HAGH hydroxyacylglutathione hydrolase 3029 138760 Nervous System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG4365 - FBgn0037024 CG4365 53290 HMC03506
HADHA hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit 3030 600890 Musculoskeletal Diseases, Digestive System Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 Mtpalpha Mitochondrial trifunctional protein alpha subunit FBgn0028479 CG4389 32873 HMS00660
HADHB hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit 3032 143450 Musculoskeletal Diseases, Digestive System Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 Thiolase Thiolase FBgn0025352 CG4581 34546 HMS01017
HARS histidyl-tRNA synthetase 3035 142810 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Aats-his Histidyl-tRNA synthetase FBgn0027087 CG6335 51485 HMC03232
HCCS holocytochrome c synthase 3052 300056 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Cchl Cytochrome c heme lyase FBgn0038925 CG6022 HMC02439
HGD homogentisate 1,2-dioxygenase 3081 607474 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 hgo homogentisate 1,2-dioxygenase FBgn0040211 CG4779 HMC03775
HIP1 huntingtin interacting protein 1 3092 601767 Neoplasms, Male Urogenital Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 Hip1 Huntingtin interacting protein 1 FBgn0036309 CG10971 38377 HMS01846
HMGCL 3-hydroxymethyl-3-methylglutaryl-CoA lyase 3155 613898 Digestive System Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CG10399 - FBgn0031877 CG10399 51861 HMC03435
HMGCR 3-hydroxy-3-methylglutaryl-CoA reductase 3156 142910 Cardiovascular Diseases, Trait 9 Hmgcr HMG Coenzyme A reductase FBgn0263782 CG10367 50652 HMC03053
HPD 4-hydroxyphenylpyruvate dioxygenase 3242 609695 Digestive System Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CG11796 - FBgn0036992 CG11796 52923 HMC03663
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD) 3248 601688 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Pdh Photoreceptor dehydrogenase FBgn0011693 CG4899
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4 3295 601860 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases, Pathological Conditions, Signs and Symptoms 9 Mfe2 peroxisomal Multifunctional enzyme type 2 FBgn0030731 CG3415 51854 HMC03428
HSPD1 heat shock 60kDa protein 1 (chaperonin) 3329 118190 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Hsp60 Heat shock protein 60 FBgn0015245 CG12101 34729 HMS01209
IDH3B isocitrate dehydrogenase 3 (NAD+) beta 3420 604526 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG6439 - FBgn0038922 CG6439 44475 HMC02361
IDS iduronate 2-sulfatase 3423 300823 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 CG12014 - FBgn0035445 CG12014 51901 HMC03475
IDUA iduronidase, alpha-L- 3425 252800 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 CG6201 - FBgn0032343 CG6201
IGBP1 immunoglobulin (CD79A) binding protein 1 3476 300139 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Tap42 Two A-associated protein of 42kDa FBgn0051852 CG31852 HMC03769
IGF1R insulin-like growth factor 1 receptor 3480 147370 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 8 InR Insulin-like receptor FBgn0013984 CG18402 51518 HMS03166
IMPDH1 IMP (inosine 5'-monophosphate) dehydrogenase 1 3614 146690 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 ras raspberry FBgn0003204 CG1799 51717 HMC03250
ITGA6 integrin, alpha 6 3655 147556 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 7 mew multiple edematous wings FBgn0004456 CG1771 44553 HMS02849
ITGA7 integrin, alpha 7 3679 600536 Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7 mew multiple edematous wings FBgn0004456 CG1771 44553 HMS02849
ITPA inosine triphosphatase (nucleoside triphosphate pyrophosphatase) 3704 147520 Nutritional and Metabolic Diseases 10 CG8891 - FBgn0031663 CG8891 51859 HMC03433
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1 3708 147265 Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Itp-r83A Inositol 1,4,5,-tris-phosphate receptor FBgn0010051 CG1063 51795 HMC03351
IVD isovaleryl-CoA dehydrogenase 3712 607036 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG6638 - FBgn0035911 CG6638
JAK2 Janus kinase 2 3717 147796 Neoplasms, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Immune System Diseases 7 hop hopscotch FBgn0004864 CG1594 32966 HMS00761
KARS lysyl-tRNA synthetase 3735 601421 Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Aats-lys Lysyl-tRNA synthetase FBgn0027084 CG12141 32967 HMS00763
KCNA1 potassium voltage-gated channel, shaker-related subfamily, member 1 (episodic ataxia with myokymia) 3736 176260 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Sh Shaker FBgn0003380 CG12348 53347 HMC03576
KCNMA1 potassium large conductance calcium-activated channel, subfamily M, alpha member 1 3778 600150 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 slo slowpoke FBgn0003429 CG10693 HMC04093
KHK ketohexokinase (fructokinase) 3795 614058 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CG7328 - FBgn0036942 CG7328 53675 HMC03664
KRAS v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog 3845 190070 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 9 Ras85D Ras oncogene at 85D FBgn0003205 CG9375 34619 HMS01294
LAMB1 laminin, beta 1 3912 150240 Musculoskeletal Diseases, Respiratory Tract Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 LanB1 LanB1 FBgn0261800 CG7123 42616 HMS02451
LAMB2 laminin, beta 2 (laminin S) 3913 150325 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 LanB1 LanB1 FBgn0261800 CG7123 42616 HMS02451
RPSA ribosomal protein SA 3921 150370 Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 sta stubarista FBgn0003517 CG14792
LDHA lactate dehydrogenase A 3939 150000 Musculoskeletal Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 ImpL3 Ecdysone-inducible gene L3 FBgn0001258 CG10160 33640 HMS00039
LDHB lactate dehydrogenase B 3945 150100 Nutritional and Metabolic Diseases 9 ImpL3 Ecdysone-inducible gene L3 FBgn0001258 CG10160 33640 HMS00039
LHCGR luteinizing hormone/choriogonadotropin receptor 3973 152790 Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 9 Lgr1 Leucine-rich repeat-containing G protein-coupled receptor 1 FBgn0016650 CG7665 51465 HMC03205
LIG1 ligase I, DNA, ATP-dependent 3978 126391 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 DNA-ligI DNA ligase I FBgn0262619 CG5602 34564, 52951 HMS01036, HMJ21620
LIG4 ligase IV, DNA, ATP-dependent 3981 601837 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Immune System Diseases 10 Lig4 Ligase4 FBgn0030506 CG12176 51933 HMC03211
LMAN1 lectin, mannose-binding, 1 3998 601567 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 ergic53 ergic53 FBgn0035909 CG6822 HMC03809
LMNB1 lamin B1 4001 150340 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Lam Lamin FBgn0002525 CG6944 57501 HMC04816
LRP4 low density lipoprotein receptor-related protein 4 4038 604270 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG8909 - FBgn0030706 CG8909 51788 HMC03344
LRP5 low density lipoprotein receptor-related protein 5 4041 603506 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 8 arr arrow FBgn0000119 CG5912 53342 HMC03571
LYZ lysozyme 4069 153450 Digestive System Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 9 LysP Lysozyme P FBgn0004429 CG9116 HMC03743
MAN2B1 mannosidase, alpha, class 2B, member 1 4125 609458 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 8 LManII Lysosomal alpha-mannosidase II FBgn0027611 CG6206 53294 HMC03510
MANBA mannosidase, beta A, lysosomal 4126 609489 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases, Mental Disorders 9 beta-Man beta-Mannosidase FBgn0037215 CG12582 53272 HMC03488
MAX MYC associated factor X 4149 154950 Neoplasms, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Max Max FBgn0017578 CG9648 40851 HMS02018
MCM6 minichromosome maintenance complex component 6 4175 601806 Digestive System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Trait 10 Mcm6 Minichromosome maintenance 6 FBgn0025815 CG4039 52111 HMC03356
MEN1 multiple endocrine neoplasia I 4221 613733 Neoplasms, Digestive System Diseases, Stomatognathic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Mnn1 Menin 1 FBgn0031885 CG13778 51862 HMC03436
MLH1 mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli) 4292 120436 Neoplasms, Digestive System Diseases, Stomatognathic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Mlh1 Mlh1 FBgn0011659 CG11482 32940 HMS00734
ALDH6A1 aldehyde dehydrogenase 6 family, member A1 4329 603178 Nutritional and Metabolic Diseases 9 CG17896 - FBgn0023537 CG17896 HMC04010
MPI mannose phosphate isomerase 4351 154550 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 10 CG8417 - FBgn0037744 CG8417 34379 HMS01369
MPV17 MpV17 mitochondrial inner membrane protein 4358 137960 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Immune System Diseases 9 CG11077 - FBgn0039930 CG11077 HMC04110
MRE11A MRE11 meiotic recombination 11 homolog A (S. cerevisiae) 4361 600814 Nervous System Diseases, Pathological Conditions, Signs and Symptoms 10 mre11 meiotic recombination 11 FBgn0020270 CG16928 39028, 50628 HMS01947, HMC02995
MSH2 mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli) 4436 609309 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 spel1 spellchecker1 FBgn0015546 CG4215 HMJ02225
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase 4522 172460 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Pathological Conditions, Signs and Symptoms 10 pug pugilist FBgn0020385 CG4067 42950, 53291 HMC03507, HMS02643
MTTP microsomal triglyceride transfer protein 4547 157147 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 Mtp Microsomal triacylglycerol transfer protein FBgn0266369 CG9342 51872 HMC03446
MUSK muscle, skeletal, receptor tyrosine kinase 4593 601296 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 8 Nrk Neurospecific receptor kinase FBgn0020391 CG4007 HMC04375, HMC03875
MYO5A myosin VA (heavy chain 12, myoxin) 4644 160777 Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 9 didum dilute class unconventional myosin FBgn0261397 CG2146 HMC03900
MYO7A myosin VIIA 4647 276903 Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Pathological Conditions, Signs and Symptoms 9 ck crinkled FBgn0000317 CG7595 41690 HMS02254
NAGLU N-acetylglucosaminidase, alpha 4669 609701 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases, Mental Disorders 10 CG13397 - FBgn0014417 CG13397 51808 HMC03368
NDUFA2 NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2, 8kDa 4695 602137 Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 10 ND-B8 NADH dehydrogenase (ubiquinone) B8 subunit FBgn0040705 CG15434 52913 HMC03653
NDUFA9 NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 9, 39kDa 4704 603834 Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 7 ND-39 NADH dehydrogenase (ubiquinone) 39 kDa subunit FBgn0037001 CG6020 52922 HMC03662
NF2 neurofibromin 2 (merlin) 4771 607379 Neoplasms, Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 8 Mer Merlin FBgn0086384 CG14228 34958 HMS00459
PNP purine nucleoside phosphorylase 4860 164050 Neoplasms, Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Immune System Diseases 9 CG16758 - FBgn0035348 CG16758 HMC02358
NPC1 Niemann-Pick disease, type C1 4864 607623 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Immune System Diseases, Mental Disorders 10 Npc1a Niemann-Pick type C-1a FBgn0024320 CG5722 37504 HMS01646
SLC11A2 solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 4891 600523 Digestive System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Mvl Malvolio FBgn0011672 CG3671 HMC04003
NT5E 5'-nucleotidase, ecto (CD73) 4907 129190 Musculoskeletal Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 veil veil FBgn0034225 CG4827 HMC03891
NT5E 5'-nucleotidase, ecto (CD73) 4907 129190 Musculoskeletal Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 NT5E-2 Ecto-5'-nucleotidase 2 FBgn0050104 CG30104 HMC03869
OAT ornithine aminotransferase 4942 613349 Musculoskeletal Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Oat Ornithine aminotransferase precursor FBgn0022774 CG8782 51481 HMC03226
OCRL oculocerebrorenal syndrome of Lowe 4952 300535 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 8 Ocrl Oculocerebrorenal syndrome of Lowe ortholog (H. sapiens) FBgn0023508 CG3573 34722 HMS01201
ODC1 ornithine decarboxylase 1 4953 165640 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Odc1 Ornithine decarboxylase 1 FBgn0013307 CG8721
OGDH oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) 4967 613022 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 Nc73EF Neural conserved at 73EF FBgn0010352 CG11661 33686 HMS00554
OGG1 8-oxoguanine DNA glycosylase 4968 601982 Neoplasms, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications 10 Ogg1 Ogg1 FBgn0027864 CG1795 51852 HMC03426
OPA1 optic atrophy 1 (autosomal dominant) 4976 605290 Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Pathological Conditions, Signs and Symptoms 10 Opa1 Optic atrophy 1 ortholog (H. sapiens) FBgn0261276 CG8479 32358 HMS00349
ORC1 origin recognition complex, subunit 1 4998 601902 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms 9 Orc1 Origin recognition complex subunit 1 FBgn0022772 CG10667
ORC4 origin recognition complex, subunit 4 5000 603056 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms 10 Orc4 Origin recognition complex subunit 4 FBgn0023181 CG2917 32409 HMS00404
OXCT1 3-oxoacid CoA transferase 1 5019 601424 Nutritional and Metabolic Diseases 10 SCOT Succinyl-CoA:3-ketoacid CoA transferase FBgn0035298 CG1140 51899 HMC03473
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa) 5048 601545 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Lis-1 Lissencephaly-1 FBgn0015754 CG8440 35043 HMS01457
PAH phenylalanine hydroxylase 5053 612349 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 Hn Henna FBgn0001208 CG7399
PARK2 parkinson protein 2, E3 ubiquitin protein ligase (parkin) 5071 602544 Neoplasms, Respiratory Tract Diseases, Nervous System Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, Pathological Conditions, Signs and Symptoms 10 park parkin FBgn0041100 CG10523 37509, 38333 HMS01651, HMS01800
PAX6 paired box 6 5080 607108 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 toy twin of eyeless FBgn0019650 CG11186 33679 HMS00544
PC pyruvate carboxylase 5091 608786 Digestive System Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 PCB Pyruvate carboxylase FBgn0027580 CG1516 HMC04104
PCK1 phosphoenolpyruvate carboxykinase 1 (soluble) 5105 614168 Digestive System Diseases, Eye Diseases, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 8 CG10924 - FBgn0034356 CG10924 36915 HMS00200
PCK2 phosphoenolpyruvate carboxykinase 2 (mitochondrial) 5106 614095 Digestive System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 Pepck Phosphoenolpyruvate carboxykinase FBgn0003067 CG17725
PCK2 phosphoenolpyruvate carboxykinase 2 (mitochondrial) 5106 614095 Digestive System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 8 CG10924 - FBgn0034356 CG10924 36915 HMS00200
PDE4D phosphodiesterase 4D, cAMP-specific 5144 600129 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases, Pathological Conditions, Signs and Symptoms 8 dnc dunce FBgn0000479 CG32498 53344 HMC03573
PDHA1 pyruvate dehydrogenase (lipoamide) alpha 1 5160 300502 Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 l(1)G0334 lethal (1) G0334 FBgn0028325 CG7010 HMC04032
PDHB pyruvate dehydrogenase (lipoamide) beta 5162 179060 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG11876 - FBgn0039635 CG11876 HMC03762
SLC25A3 solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3 5250 600370 Nutritional and Metabolic Diseases 9 Mpcp Mitochondrial phosphate carrier protein FBgn0026409 CG4994 44508 HMC02898
SLC25A3 solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3 5250 600370 Nutritional and Metabolic Diseases 10 CG9090 - FBgn0034497 CG9090 44495 HMC02425
PHKA2 phosphorylase kinase, alpha 2 (liver) 5256 300798 Digestive System Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG7766 - FBgn0030087 CG7766 42890 HMS02583
PHKB phosphorylase kinase, beta 5257 172490 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG8475 - FBgn0031995 CG8475 34904 HMS01249
PIGA phosphatidylinositol glycan anchor biosynthesis, class A 5277 311770 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG6401 - FBgn0034270 CG6401 51882 HMC03456
PMM2 phosphomannomutase 2 5373 601785 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases, Immune System Diseases 10 CG10688 - FBgn0036300 CG10688 51905, 42956 HMC03480, HMS02649
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae) 5395 600259 Neoplasms, Digestive System Diseases, Stomatognathic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Pms2 Pms2 FBgn0011660 CG8169 HMC03753
POLA1 polymerase (DNA directed), alpha 1, catalytic subunit 5422 312040 Neoplasms, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 DNApol-alpha180 DNA polymerase alpha 180kD FBgn0259113 CG6349 53341 HMC03570
POLG polymerase (DNA directed), gamma 5428 174763 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Endocrine System Diseases, Mental Disorders 9 tam tamas FBgn0004406 CG8987
POLH polymerase (DNA directed), eta 5429 603968 Eye Diseases, Skin and Connective Tissue Diseases 9 DNApol-eta DNApol-eta FBgn0037141 CG7143 33410 HMS00290
POR P450 (cytochrome) oxidoreductase 5447 124015 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Endocrine System Diseases 10 Cpr Cytochrome P450 reductase FBgn0015623 CG11567 51809 HMC03369
PPIB peptidylprolyl isomerase B (cyclophilin B) 5479 123841 Musculoskeletal Diseases, Stomatognathic Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG2852 - FBgn0034753 CG2852 HMC03892
PPOX protoporphyrinogen oxidase 5498 600923 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Ppox Protoporphyrinogen oxidase FBgn0020018 CG5796 51777 HMC03332
PPT1 palmitoyl-protein thioesterase 1 5538 600722 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Ppt1 Palmitoyl-protein thioesterase 1 FBgn0030057 CG12108 HMC04018
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha (tissue specific extinguisher 1) 5573 188830 Neoplasms, Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Endocrine System Diseases, Mental Disorders 8 Pka-R1 cAMP-dependent protein kinase R1 FBgn0259243 CG42341 52906 HMC03646
PRKCA protein kinase C, alpha 5578 176960 Neoplasms, Nervous System Diseases, Endocrine System Diseases 10 Pkc53E Protein C kinase 53E FBgn0003091 CG6622 34716 HMS01195, HMC04134
PRKCSH protein kinase C substrate 80K-H 5589 177060 Musculoskeletal Diseases, Digestive System Diseases, Respiratory Tract Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 GCS2beta Glucosidase 2 beta subunit FBgn0032643 CG6453 35008 HMS01418
MAPK10 mitogen-activated protein kinase 10 5602 602897 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 8 bsk basket FBgn0000229 CG5680 32977, 53310, 57035 HMC03539, HMS00777, HMS04479
MAP2K1 mitogen-activated protein kinase kinase 1 5604 176872 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Dsor1 Downstream of raf1 FBgn0010269 CG15793 33639, 34830, 32920 HMS00037, HMS00145, HMS00710
MAP2K2 mitogen-activated protein kinase kinase 2 5605 601263 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Dsor1 Downstream of raf1 FBgn0010269 CG15793 33639, 34830, 32920 HMS00037, HMS00145, HMS00710
PRODH proline dehydrogenase (oxidase) 1 5625 606810 Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 10 slgA sluggish A FBgn0003423 CG1417 51811 HMC03382
PSEN1 presenilin 1 5663 104311 Bacterial Infections and Mycoses, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 9 Psn Presenilin FBgn0019947 CG18803 38374 HMS01843
PSPH phosphoserine phosphatase 5723 172480 Nutritional and Metabolic Diseases 10 aay astray FBgn0023129 CG3705 38338 HMS01805
PTCH1 patched 1 5727 601309 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms 9 ptc patched FBgn0003892 CG2411 HMC03872
PTEN phosphatase and tensin homolog 5728 601728 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases, Pathological Conditions, Signs and Symptoms, Mental Disorders 10 Pten Pten FBgn0026379 CG5671 33643 HMS00044
PTPN11 protein tyrosine phosphatase, non-receptor type 11 5781 176876 Neoplasms, Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 9 csw corkscrew FBgn0000382 CG3954 33619 HMS00012
PTS 6-pyruvoyltetrahydropterin synthase 5805 612719 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Mental Disorders 9 pr purple FBgn0003141 CG16784 53346 HMC03575
PEX2 peroxisomal biogenesis factor 2 5828 170993 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Pex2 Peroxin 2 FBgn0035876 CG7081
PEX5 peroxisomal biogenesis factor 5 5830 600414 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Pex5 Peroxin 5 FBgn0023516 CG14815 42854, 58064 HMC04009, HMS02546, HMJ21920
ALDH18A1 aldehyde dehydrogenase 18 family, member A1 5832 138250 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG7470 - FBgn0037146 CG7470 51911 HMC03487
PYGM phosphorylase, glycogen, muscle 5837 608455 Musculoskeletal Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 GlyP Glycogen phosphorylase FBgn0004507 CG7254 33634 HMS00032
QDPR quinoid dihydropteridine reductase 5860 612676 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Mental Disorders 10 Dhpr Dihydropteridine reductase FBgn0035964 CG4665
RAB27A RAB27A, member RAS oncogene family 5873 603868 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 Rab27 Rab27 FBgn0025382 CG14791 35774 HMS01523
RAD51 RAD51 homolog (S. cerevisiae) 5888 179617 Neoplasms, Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 spn-A spindle A FBgn0003479 CG7948 50988, 51926 HMC03364, HMJ21099
RAP1GDS1 RAP1, GTP-GDP dissociation stimulator 1 5910 179502 Neoplasms, Hemic and Lymphatic Diseases, Immune System Diseases 10 vimar visceral mesodermal armadillo-repeats FBgn0022960 CG3572 32951, 41996 HMS00745, HMS02397
RAPSN receptor-associated protein of the synapse 5913 601592 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 CG1909 - FBgn0039911 CG1909 44538 HMC02933
RASA1 RAS p21 protein activator (GTPase activating protein) 1 5921 139150 Neoplasms, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Pathological Conditions, Signs and Symptoms 10 vap vacuolar peduncle FBgn0003969 CG9209 51793 HMC03349
RPL11 ribosomal protein L11 6135 604175 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 RpL11 Ribosomal protein L11 FBgn0013325 CG7726
ETFB electron-transfer-flavoprotein, beta polypeptide 2109 130410 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG7834 - FBgn0039697 CG7834 51464 HMC03204
ETFDH electron-transferring-flavoprotein dehydrogenase 2110 231675 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 Etf-QO Electron transfer flavoprotein-ubiquinone oxidoreductase FBgn0033465 CG12140 HMC03516
MECOM MDS1 and EVI1 complex locus 2122 165215 Neoplasms, Hemic and Lymphatic Diseases 8 ham hamlet FBgn0045852 CG31753 32470 HMS00470
EXT1 exostosin 1 2131 608177 Neoplasms, Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 ttv tout-velu FBgn0265974 CG10117 51480 HMC03225
EXT2 exostosin 2 2132 608210 Neoplasms, Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 Ext2 Ext2 FBgn0029175 CG8433 52883 HMC03621
EZH2 enhancer of zeste homolog 2 (Drosophila) 2146 601573 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 E(z) Enhancer of zeste FBgn0000629 CG6502 33659 HMS00066
FANCD2 Fanconi anemia, complementation group D2 2177 613984 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 Fancd2 Fancd2 FBgn0038827 CG17269 53329 HMC04180, HMC03558
ACSL4 acyl-CoA synthetase long-chain family member 4 2182 300157 Nervous System Diseases, Pathological Conditions, Signs and Symptoms 9 Acsl Acyl-CoA synthetase long-chain FBgn0263120 CG8732 41885 HMS02307
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase) 2184 613871 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Immune System Diseases 10 Faa Fumarylacetoacetase FBgn0016013 CG14993 51796 HMC03352
FBP1 fructose-1,6-bisphosphatase 1 2203 611570 Digestive System Diseases, Respiratory Tract Diseases, Nervous System Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Mental Disorders 10 fbp fructose-1,6-bisphosphatase FBgn0032820 CG31692 51871 HMC03445
FECH ferrochelatase 2235 612386 Digestive System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 FeCH Ferrochelatase FBgn0266268 CG2098 HMC03757
FH fumarate hydratase 2271 136850 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 l(1)G0255 lethal (1) G0255 FBgn0028336 CG4094 51779 HMC03334
FLNA filamin A, alpha 2316 300017 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms 10 cher cheerio FBgn0014141 CG3937 35755 HMS01501
KDSR 3-ketodihydrosphingosine reductase 2531 136440 Neoplasms, Hemic and Lymphatic Diseases, Immune System Diseases 10 CG10425 - FBgn0039304 CG10425
NDUFA10 NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 10, 42kDa 4705 603835 Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 9 ND-42 NADH dehydrogenase (ubiquinone) 42 kDa subunit FBgn0019957 CG6343 34526, 32998 HMS00852, HMS00798
NDUFS1 NADH dehydrogenase (ubiquinone) Fe-S protein 1, 75kDa (NADH-coenzyme Q reductase) 4719 157655 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 ND-75 NADH dehydrogenase (ubiquinone) 75 kDa subunit FBgn0017566 CG2286 33911, 33910 HMS00853, HMS00854
NDUFS2 NADH dehydrogenase (ubiquinone) Fe-S protein 2, 49kDa (NADH-coenzyme Q reductase) 4720 602985 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 ND-49 NADH dehydrogenase (ubiquinone) 49 kDa subunit FBgn0039909 CG1970 57499 HMC04814
NDUFS3 NADH dehydrogenase (ubiquinone) Fe-S protein 3, 30kDa (NADH-coenzyme Q reductase) 4722 603846 Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 9 ND-30 NADH dehydrogenase (ubiquinone) 30 kDa subunit FBgn0266582 CG12079 51425, 44535 HMC02895, HMC02929
NDUFV1 NADH dehydrogenase (ubiquinone) flavoprotein 1, 51kDa 4723 161015 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 9 ND-51 NADH dehydrogenase (ubiquinone) 51 kDa subunit FBgn0031771 CG9140 36701, 52939 HMJ21591, HMS01590
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase) 4724 602694 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 9 ND-18 NADH dehydrogenase (ubiquinone) 18 kDa subunit FBgn0031021 CG12203 53325 HMC03554
NDUFS6 NADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kDa (NADH-coenzyme Q reductase) 4726 603848 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 ND-13A NADH dehydrogenase (ubiquinone) 13 kDa A subunit FBgn0031684 CG8680 51860 HMC03434
NDUFS8 NADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kDa (NADH-coenzyme Q reductase) 4728 602141 Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 10 ND-23 NADH dehydrogenase (ubiquinone) 23 kDa subunit FBgn0017567 CG3944 51797 HMC03353
NDUFV2 NADH dehydrogenase (ubiquinone) flavoprotein 2, 24kDa 4729 600532 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 ND-24 NADH dehydrogenase (ubiquinone) 24 kDa subunit FBgn0030853 CG5703 51855 HMC03429
NF1 neurofibromin 1 4763 613113 Neoplasms, Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Nf1 Neurofibromin 1 FBgn0015269 CG8318 53322 HMC03551
PEPD peptidase D 5184 613230 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 Dip-C Dipeptidase C FBgn0000455 CG5663 51708 HMC03216
PEX7 peroxisomal biogenesis factor 7 5191 601757 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Pex7 Peroxin 7 FBgn0035922 CG6486
PEX10 peroxisomal biogenesis factor 10 5192 602859 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Pex10 Peroxin 10 FBgn0035233 CG7864 51826 HMC03398
PEX12 peroxisomal biogenesis factor 12 5193 601758 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Pex12 Peroxin 12 FBgn0031282 CG3639 53308 HMC03536
PEX13 peroxisomal biogenesis factor 13 5194 601789 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 9 Pex13 Peroxin 13 FBgn0033812 CG4663 50697 HMC03099
PEX14 peroxisomal biogenesis factor 14 5195 601791 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Pex14 Peroxin 14 FBgn0037020 CG4289
PFKM phosphofructokinase, muscle 5213 610681 Musculoskeletal Diseases, Digestive System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Pfk Phosphofructokinase FBgn0003071 CG4001 34336 HMS01324
PGAM2 phosphoglycerate mutase 2 (muscle) 5224 612931 Musculoskeletal Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Pglym87 Pglym87 FBgn0011270 CG17645 51939 HMC03367
PGAM2 phosphoglycerate mutase 2 (muscle) 5224 612931 Musculoskeletal Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 Pglym78 Phosphoglyceromutase FBgn0014869 CG1721 57503 HMC04818
PGK1 phosphoglycerate kinase 1 5230 311800 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 10 Pgk Phosphoglycerate kinase FBgn0250906 CG3127 33633, 33632 HMS00030, HMS00031
PGM1 phosphoglucomutase 1 5236 171900 Musculoskeletal Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Pgm phosphoglucose mutase FBgn0003076 CG5165 34345 HMS01333
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 5243 171050 Digestive System Diseases, Disease risk factor, diagnosis or treatment 8 Mdr50 Multi drug resistance 50 FBgn0010241 CG8523 35034 HMS01448
PHB prohibitin 5245 176705 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 l(2)37Cc lethal (2) 37Cc FBgn0002031 CG10691 32912, 32404 HMS00399, HMS00702
RPL35A ribosomal protein L35a 6165 180468 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 RpL35A Ribosomal protein L35A FBgn0037328 CG2099
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3 6197 300075 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms 9 S6kII Ribosomal protein S6 kinase II FBgn0262866 CG17596 51694 HMC03140, HMC04339
RPS7 ribosomal protein S7 6201 603658 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 RpS7 Ribosomal protein S7 FBgn0039757 CG1883
RPS10 ribosomal protein S10 6204 603632 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 RpS10b Ribosomal protein S10b FBgn0261593 CG14206
RPS17 ribosomal protein S17 6218 180472 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 RpS17 Ribosomal protein S17 FBgn0005533 CG3922 42656 HMS02492
RPS19 ribosomal protein S19 6223 603474 Neoplasms, Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 RpS19b Ribosomal protein S19b FBgn0039129 CG5338 HMC03825
RPS26 ribosomal protein S26 6231 603701 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 RpS26 Ribosomal protein S26 FBgn0261597 CG10305 33393 HMS00270
RYR2 ryanodine receptor 2 (cardiac) 6262 180902 Cardiovascular Diseases, Pathological Conditions, Signs and Symptoms 9 RyR Ryanodine receptor FBgn0011286 CG10844
ATXN2 ataxin 2 6311 601517 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 7 Atx2 Ataxin-2 FBgn0041188 CG5166 36114, 44012 HMS01392, HMS02726
SCO1 SCO cytochrome oxidase deficient homolog 1 (yeast) 6341 603644 Digestive System Diseases 10 Scox Synthesis of cytochrome c oxidase FBgn0262467 CG8885 HMC03860
SCP2 sterol carrier protein 2 6342 184755 Nervous System Diseases 9 ScpX Sterol carrier protein X-related thiolase FBgn0015808 CG17320 51479 HMC03224
SCP2 sterol carrier protein 2 6342 184755 Nervous System Diseases 9 CG17597 - FBgn0032715 CG17597 52886 HMC03624
SDHA succinate dehydrogenase complex, subunit A, flavoprotein (Fp) 6389 600857 Neoplasms, Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 10 SdhA Succinate dehydrogenase, subunit A (flavoprotein) FBgn0261439 CG17246
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip) 6390 185470 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 SdhB Succinate dehydrogenase, subunit B (iron-sulfur) FBgn0014028 CG3283
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa 6391 602413 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 SdhC Succinate dehydrogenase, subunit C FBgn0037873 CG6666 53281 HMC03497
TRAPPC2 trafficking protein particle complex 2 6399 300202 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Trs20 TRAPP subunit 20 ortholog (S. cerevisiae) FBgn0266724 CG5161 53328 HMC03557
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein) 6444 601411 Musculoskeletal Diseases, Nervous System Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Scgdelta Sarcoglycan delta FBgn0025391 CG14808 HMC04012
SGSH N-sulfoglucosamine sulfohydrolase 6448 605270 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 CG14291 - FBgn0038660 CG14291
SHH sonic hedgehog 6469 600725 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 hh hedgehog FBgn0004644 CG4637 32489 HMS00492
SLC3A1 solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1 6519 104614 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Endocrine System Diseases, Mental Disorders 8 Mal-B1 Maltase B1 FBgn0032381 CG14934 HMC04033
SLC3A1 solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1 6519 104614 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Endocrine System Diseases, Mental Disorders 7 Mal-A8 Maltase A8 FBgn0033297 CG8690 HMC03889
SLC3A1 solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1 6519 104614 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Endocrine System Diseases, Mental Disorders 8 Mal-A5 Maltase A5 FBgn0050359 CG30359 52910 HMC03650, HMJ21242
SLC6A2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 6530 163970 Nervous System Diseases, Pathological Conditions, Signs and Symptoms 9 DAT Dopamine transporter FBgn0034136 CG8380 50619 HMC02986
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 6597 603254 Neoplasms, Nervous System Diseases, Pathological Conditions, Signs and Symptoms 10 brm brahma FBgn0000212 CG5942 34520 HMS00050
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 6598 601607 Neoplasms, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Pathological Conditions, Signs and Symptoms 10 Snr1 Snf5-related 1 FBgn0011715 CG1064 32372 HMS00363
SMO smoothened, frizzled family receptor 6608 601500 Neoplasms 9 smo smoothened FBgn0003444 CG11561 53348 HMC03577
SMPD1 sphingomyelin phosphodiesterase 1, acid lysosomal 6609 607608 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 CG3376 - FBgn0034997 CG3376 36760 HMS03021
SMS spermine synthase 6611 300105 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 CG4300 - FBgn0036272 CG4300 52924 HMC03665
SOD1 superoxide dismutase 1, soluble 6647 147450 Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Sod Superoxide dismutase FBgn0003462 CG11793 32909, 34616 HMS01291, HMS00698
SOD2 superoxide dismutase 2, mitochondrial 6648 147460 Nutritional and Metabolic Diseases, Endocrine System Diseases 9 Sod2 Superoxide dismutase 2 (Mn) FBgn0010213 CG8905 32983, 32496 HMS00499, HMS00783
SORD sorbitol dehydrogenase 6652 182500 Eye Diseases 9 Sodh-2 Sorbitol dehydrogenase-2 FBgn0022359 CG4649 53353 HMC03582
SORD sorbitol dehydrogenase 6652 182500 Eye Diseases 10 Sodh-1 Sorbitol dehydrogenase 1 FBgn0024289 CG1982 34556 HMS01028
SOS1 son of sevenless homolog 1 (Drosophila) 6654 182530 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Sos Son of sevenless FBgn0001965 CG7793 34833 HMS00149
SPAST spastin 6683 604277 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 spas spastin FBgn0039141 CG5977 53331 HMC03560
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive) 6687 602783 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 CG2658 - FBgn0024992 CG2658 HMC04011
SPR sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase) 6697 182125 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 10 Sptr Sepiapterin reductase FBgn0014032 CG12117 HMC04004
SPTAN1 spectrin, alpha, non-erythrocytic 1 6709 182810 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases 10 alpha-Spec alpha Spectrin FBgn0250789 CG1977 HMC04371
STIM1 stromal interaction molecule 1 6786 605921 Musculoskeletal Diseases, Stomatognathic Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Immune System Diseases 9 Stim Stromal interaction molecule FBgn0045073 CG9126 52911 HMC03651
STK11 serine/threonine kinase 11 6794 602216 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 9 lkb1 lkb1 FBgn0038167 CG9374 34362 HMS01351
STXBP1 syntaxin binding protein 1 6812 602926 Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Rop Ras opposite FBgn0004574 CG15811 51925 HMC03422
SUOX sulfite oxidase 6821 606887 Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG7280 - FBgn0030966 CG7280
SURF1 surfeit 1 6834 185620 Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 10 Surf1 Surfeit 1 FBgn0029117 CG9943 51783 HMC03338
ADAM17 ADAM metallopeptidase domain 17 6868 603639 Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Skin and Connective Tissue Diseases, Immune System Diseases 9 Tace Tace FBgn0039734 CG7908
TACR3 tachykinin receptor 3 6870 162332 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Skin and Connective Tissue Diseases, Endocrine System Diseases 7 TkR99D Tachykinin-like receptor at 99D FBgn0004622 CG7887 HMC03749
TAF1 TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa 6872 313650 Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Taf1 TBP-associated factor 1 FBgn0010355 CG17603 32421 HMS00416
TALDO1 transaldolase 1 6888 602063 Nutritional and Metabolic Diseases 10 Tal Tal FBgn0023477 CG2827 51709 HMC03227
TAT tyrosine aminotransferase 6898 613018 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG1461 - FBgn0030558 CG1461 51470 HMC03212
TAZ tafazzin 6901 300394 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Immune System Diseases 10 Taz Tafazzin FBgn0026619 CG8766 51484 HMC03231
TBP TATA box binding protein 6908 600075 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 8 Tbp TATA binding protein FBgn0003687 CG9874 HMC04197
TEAD1 TEA domain family member 1 (SV40 transcriptional enhancer factor) 7003 189967 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 sd scalloped FBgn0003345 CG8544 HMC04092
TGFBI transforming growth factor, beta-induced, 68kDa 7045 601692 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 mfas midline fasciclin FBgn0260745 CG3359 52905 HMC03645, HMJ22320, HMJ22563
TGFBR1 transforming growth factor, beta receptor 1 7046 190181 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 8 babo baboon FBgn0011300 CG8224 40866 HMS02033, HMC04142
TGM1 transglutaminase 1 (K polypeptide epidermal type I, protein-glutamine-gamma-glutamyltransferase) 7051 190195 Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Tg Transglutaminase FBgn0031975 CG7356
TH tyrosine hydroxylase 7054 191290 Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 7 ple pale FBgn0005626 CG10118
TK2 thymidine kinase 2, mitochondrial 7084 188250 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Immune System Diseases 8 dnk deoxyribonucleoside kinase FBgn0022338 CG5452
TOP1 topoisomerase (DNA) I 7150 126420 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 Top1 Topoisomerase 1 FBgn0004924 CG6146 HMC04001
TPI1 triosephosphate isomerase 1 7167 190450 Musculoskeletal Diseases, Digestive System Diseases, Nervous System Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Tpi Triose phosphate isomerase FBgn0086355 CG2171 51829 HMC03401
TSC1 tuberous sclerosis 1 7248 605284 Neoplasms, Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases, Immune System Diseases, Mental Disorders 9 Tsc1 Tsc1 FBgn0026317 CG6147 54034, 52931 HMC03672, HMJ21085, HMJ21477
TSC2 tuberous sclerosis 2 7249 191092 Neoplasms, Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases, Immune System Diseases, Mental Disorders 10 gig gigas FBgn0005198 CG6975 34737 HMS01217
TSG101 tumor susceptibility gene 101 7251 601387 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 TSG101 Tumor susceptibility gene 101 FBgn0036666 CG9712 38306 HMS01768
TUFM Tu translation elongation factor, mitochondrial 7284 602389 Nutritional and Metabolic Diseases 10 EfTuM Elongation factor Tu mitochondrial FBgn0024556 CG6050 32868 HMS00655
UBA1 ubiquitin-like modifier activating enzyme 1 7317 314370 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Uba1 Ubiquitin activating enzyme 1 FBgn0023143 CG1782
UBE2A ubiquitin-conjugating enzyme E2A 7319 312180 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms 10 Ubc6 Ubiquitin conjugating enzyme 6 FBgn0004436 CG2013 42631 HMS02466
UBE2B ubiquitin-conjugating enzyme E2B 7320 179095 Male Urogenital Diseases 9 Ubc6 Ubiquitin conjugating enzyme 6 FBgn0004436 CG2013 42631 HMS02466
UBE3A ubiquitin protein ligase E3A 7337 601623 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 10 Ube3a Ubiquitin protein ligase E3A FBgn0061469 CG6190 57151 HMC04528
UMPS uridine monophosphate synthetase 7372 613891 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 r-l rudimentary-like FBgn0003257 CG3593 HMC03871
UQCRB ubiquinol-cytochrome c reductase binding protein 7381 191330 Musculoskeletal Diseases, Digestive System Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 10 UQCR-14 Ubiquinol-cytochrome c reductase 14 kDa subunit FBgn0030733 CG3560
UQCRB ubiquinol-cytochrome c reductase binding protein 7381 191330 Musculoskeletal Diseases, Digestive System Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 10 UQCR-14L Ubiquinol-cytochrome c reductase 14 kDa subunit-like FBgn0039576 CG17856 HMC03778
UROD uroporphyrinogen decarboxylase 7389 613521 Neoplasms, Digestive System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Updo Updo FBgn0033428 CG1818
UROS uroporphyrinogen III synthase 7390 606938 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 CG1885 - FBgn0030066 CG1885 51786 HMC03341
KDM6A lysine (K)-specific demethylase 6A 7403 300128 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 Utx - FBgn0260749 CG5640 34076 HMS00575
VCL vinculin 7414 193065 Cardiovascular Diseases 8 Vinc Vinculin FBgn0004397 CG3299 41959 HMS02356
VCP valosin containing protein 7415 601023 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 TER94 TER94 FBgn0261014 CG2331 32869 HMS00656
VRK1 vaccinia related kinase 1 7443 602168 Musculoskeletal Diseases, Respiratory Tract Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 ball ballchen FBgn0027889 CG6386 HMC04017
WAS Wiskott-Aldrich syndrome (eczema-thrombocytopenia) 7454 300392 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 9 WASp WASp FBgn0024273 CG1520 51802 HMC03360
WFS1 Wolfram syndrome 1 (wolframin) 7466 606201 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 9 wfs1 wolfram syndrome 1 FBgn0039003 CG4917 53330 HMC03559
XDH xanthine dehydrogenase 7498 607633 Musculoskeletal Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 ry rosy FBgn0003308 CG7642 44106, 54845 HMJ21582, HMS02827
XPA xeroderma pigmentosum, complementation group A 7507 611153 Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Xpac Xeroderma pigmentosum group A-like FBgn0004832 CG6358 51806 HMC03365
XRCC3 X-ray repair complementing defective repair in Chinese hamster cells 3 7517 600675 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 spn-B spindle B FBgn0003480 CG3325 HMC04091
CNBP CCHC-type zinc finger, nucleic acid binding protein 7555 116955 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG3800 - FBgn0034802 CG3800
MOGS mannosyl-oligosaccharide glucosidase 7841 601336 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 GCS1 Glucosidase 1 FBgn0030289 CG1597 50699 HMC03101
RAB7A RAB7A, member RAS oncogene family 7879 602298 Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 8 Rab7 Rab7 FBgn0015795 CG5915
ALDH5A1 aldehyde dehydrogenase 5 family, member A1 7915 610045 Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 9 Ssadh Succinic semialdehyde dehydrogenase FBgn0039349 CG4685 HMC03868
CCDC6 coiled-coil domain containing 6 8030 601985 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 9 CG6664 - FBgn0036685 CG6664 HMC03792
SHOC2 soc-2 suppressor of clear homolog (C. elegans) 8036 602775 Musculoskeletal Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Sur-8 Sur-8 FBgn0038504 CG5407 41883 HMS02299
AAAS achalasia, adrenocortical insufficiency, alacrimia 8086 605378 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 CG16892 - FBgn0030122 CG16892 51938 HMC03342
PABPN1 poly(A) binding protein, nuclear 1 8106 602279 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Pabp2 Pabp2 FBgn0005648 CG2163 34602 HMS00553
SMC1A structural maintenance of chromosomes 1A 8243 300040 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 SMC1 Structural maintenance of chromosomes 1 FBgn0040283 CG6057 34351 HMS01340
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit 8260 300013 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Cardiovascular Diseases, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 vnc variable nurse cells FBgn0263251 CG11989 HMJ21624, HMC03479
PICALM phosphatidylinositol binding clathrin assembly protein 8301 603025 Neoplasms, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 lap like-AP180 FBgn0086372 CG2520 39021 HMS01939, HMC02373
BAP1 BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase) 8314 603089 Neoplasms, Musculoskeletal Diseases, Respiratory Tract Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 calypso calypso FBgn0262166 CG8445 HMC04109
MAD1L1 MAD1 mitotic arrest deficient-like 1 (yeast) 8379 602686 Neoplasms, Male Urogenital Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Immune System Diseases 8 Mad1 - FBgn0026326 CG2072 52930 HMC03671
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent) 8398 603604 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 9 iPLA2-VIA calcium-independent phospholipase A2 VIA FBgn0036053 CG6718 36129 HMS01544
RAD54L RAD54-like (S. cerevisiae) 8438 603615 Neoplasms, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Immune System Diseases 9 okr okra FBgn0002989 CG3736 33707 HMS00585
GNPAT glyceronephosphate O-acyltransferase 8443 602744 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Dhap-at Dihydroxyacetone phosphate acyltransferase FBgn0040212 CG4625 52914 HMC03654
CUL4B cullin 4B 8450 300304 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Male Urogenital Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases, Mental Disorders 9 Cul4 Cullin 4 FBgn0033260 CG8711 50614 HMC02981
PEX3 peroxisomal biogenesis factor 3 8504 603164 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Pex3 Peroxin 3 FBgn0036484 CG6859 50694 HMC03096
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein 8518 603722 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 10 Elp1 Elongator complex protein 1 FBgn0037926 CG10535 HMJ21504
AGPS alkylglycerone phosphate synthase 8540 603051 Musculoskeletal Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG10253 - FBgn0033983 CG10253 34350 HMS01339
YARS tyrosyl-tRNA synthetase 8565 603623 Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Aats-tyr Tyrosyl-tRNA synthetase FBgn0027080 CG4561 HMC04013
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family) 8573 300172 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms, Mental Disorders 9 CASK CASK ortholog FBgn0013759 CG6703 32857, 51721, 57046 HMS00644, HMC03260, HMS04480
SLC25A12 solute carrier family 25 (aspartate/glutamate carrier), member 12 8604 603667 Musculoskeletal Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 aralar1 aralar1 FBgn0028646 CG2139 HMC04105
PDE8B phosphodiesterase 8B 8622 603390 Musculoskeletal Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Endocrine System Diseases, Mental Disorders 10 Pde8 Phosphodiesterase 8 FBgn0266377 CG45019 51892 HMC03466
RFXANK regulatory factor X-associated ankyrin-containing protein 8625 603200 Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 8 CG5846 - FBgn0032171 CG5846
ALDH4A1 aldehyde dehydrogenase 4 family, member A1 8659 606811 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 P5CDh1 delta-1-Pyrroline-5-carboxylate dehydrogenase 1 FBgn0037138 CG7145
STX16 syntaxin 16 8675 603666 Musculoskeletal Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 10 Syx16 Syntaxin 16 FBgn0031106 CG1467 51856 HMC03430
SUCLG1 succinate-CoA ligase, alpha subunit 8802 611224 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 Scsalpha Succinyl coenzyme A synthetase alpha subunit FBgn0004888 CG1065 51807 HMC03366
SUCLA2 succinate-CoA ligase, ADP-forming, beta subunit 8803 603921 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Immune System Diseases, Mental Disorders 9 skap skpA associated protein FBgn0037643 CG11963 HMC03847
DPM1 dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit 8813 603503 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 CG10166 - FBgn0032799 CG10166 50713 HMS02947
BANF1 barrier to autointegration factor 1 8815 603811 Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 baf barrier to autointegration factor FBgn0031977 CG7380 36108 HMS00195
EIF2B4 eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa 8890 606687 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, Mental Disorders 10 eIF2B-delta eIF2B-delta FBgn0034858 CG10315 51891 HMC03465
EIF2B3 eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa 8891 606273 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, Mental Disorders 10 eIF2B-gamma eIF2B-gamma FBgn0034029 CG8190 41948 HMS02345
EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa 8892 606454 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, Mental Disorders 9 eIF2B-beta eIF2B-beta FBgn0024996 CG2677 HMC03838
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa 8893 603945 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, Mental Disorders 10 eIF2B-epsilon eIF2B-epsilon FBgn0023512 CG3806 HMC04008
MTMR2 myotubularin related protein 2 8898 603557 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 mtm myotubularin FBgn0025742 CG9115 38339, 57298 HMS01806, HMS04495
AP1S2 adaptor-related protein complex 1, sigma 2 subunit 8905 300629 Nervous System Diseases, Pathological Conditions, Signs and Symptoms 10 AP-1sigma Adaptor Protein complex 1, sigma subunit FBgn0039132 CG5864 40895 HMS02143
SGCE sarcoglycan, epsilon 8910 604149 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 9 Scgalpha Sarcoglycan alpha FBgn0032013 CG7851 34027 HMS00997
PLOD3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 8985 603066 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Plod procollagen lysyl hydroxylase FBgn0036147 CG6199 34911 HMS01259
AIP aryl hydrocarbon receptor interacting protein 9049 605555 Neoplasms, Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Endocrine System Diseases 10 CG1847 - FBgn0030345 CG1847 44490 HMC02409
UNC119 unc-119 homolog (C. elegans) 9094 604011 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 unc-119 unc-119 FBgn0025549 CG1659 HMC03736
SMC3 structural maintenance of chromosomes 3 9126 606062 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 SMC3 Structural maintenance of chromosomes 3 FBgn0015615 CG9802 33431, 50899 HMS00318, HMJ03116
PRPF3 PRP3 pre-mRNA processing factor 3 homolog (S. cerevisiae) 9129 607301 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Prp3 Precursor RNA processing 3 FBgn0036915 CG7757 51940 HMC03485, HMC03943
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1 9131 300169 Nutritional and Metabolic Diseases 9 AIF Apoptosis inducing factor FBgn0031392 CG7263
CTDP1 CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1 9150 604927 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Fcp1 - FBgn0035026 CG12252 32925, 57021 HMS00716, HMS04464
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1 9197 603690 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG9706 - FBgn0036662 CG9706 51908 HMC03483
AIMP1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 9255 603605 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG8235 - FBgn0033351 CG8235 51874 HMC03448
SNAP29 synaptosomal-associated protein, 29kDa 9342 604202 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Snap29 Synaptosomal-associated protein 29kDa FBgn0034913 CG11173 51893 HMC03467
GRHPR glyoxylate reductase/hydroxypyruvate reductase 9380 604296 Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG1236 - FBgn0037370 CG1236 53274 HMC03490
COG1 component of oligomeric golgi complex 1 9382 606973 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG4848 - FBgn0037998 CG4848 38943 HMS01857
PEX16 peroxisomal biogenesis factor 16 9409 603360 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Pex16 Peroxin 16 FBgn0037019 CG3947 57495 HMC04810
MED23 mediator complex subunit 23 9439 605042 Nervous System Diseases, Pathological Conditions, Signs and Symptoms 10 MED23 Mediator complex subunit 23 FBgn0034795 CG3695 52871, 34658, 56970 HMC03609, HMS01135, HMC04411
MED17 mediator complex subunit 17 9440 603810 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 MED17 Mediator complex subunit 17 FBgn0038578 CG7957 34664 HMS01141
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3 9451 604032 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 9 PEK pancreatic eIF-2alpha kinase FBgn0037327 CG2087 42499 HMJ02063
SPTLC2 serine palmitoyltransferase, long chain base subunit 2 9517 605713 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 lace lace FBgn0002524 CG4162 51475 HMC03219
TECR trans-2,3-enoyl-CoA reductase 9524 610057 Nervous System Diseases, Pathological Conditions, Signs and Symptoms 10 Sc2 Sc2 FBgn0035471 CG10849 51902 HMC03476
POLR1C polymerase (RNA) I polypeptide C, 30kDa 9533 610060 Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG3756 - FBgn0031657 CG3756
MINPP1 multiple inositol-polyphosphate phosphatase 1 9562 605391 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 9 Mipp2 Multiple inositol polyphosphate phosphatase 2 FBgn0026060 CG4317 51482 HMC03229
GOSR2 golgi SNAP receptor complex member 2 9570 604027 Musculoskeletal Diseases, Nervous System Diseases 10 Membrin Membrin FBgn0260856 CG4780 HMJ21936
RB1CC1 RB1-inducible coiled-coil 1 9821 606837 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 Atg17 Autophagy-related 17 FBgn0037363 CG1347 36918 HMS01611
FIG4 FIG4 homolog, SAC1 lipid phosphatase domain containing (S. cerevisiae) 9896 609390 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG17840 - FBgn0031611 CG17840 38291, 58063 HMS01749, HMJ21919
KIAA0196 KIAA0196 9897 610657 Musculoskeletal Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications 9 CG12272 - FBgn0036571 CG12272 51906 HMC03481
MFN2 mitofusin 2 9927 608507 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Marf Mitochondrial assembly regulatory factor FBgn0029870 CG3869 HMC03883
GOLGA5 golgin A5 9950 606918 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 8 Golgin84 Golgin-84 ortholog (H. sapiens) FBgn0039188 CG17785 39039 HMS01959
ABCB6 ATP-binding cassette, sub-family B (MDR/TAP), member 6 10058 605452 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Trait 10 Hmt-1 Heavy metal tolerance factor 1 FBgn0038376 CG4225 53284 HMC03500
DNM1L dynamin 1-like 10059 603850 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 Drp1 Dynamin related protein 1 FBgn0026479 CG3210 51483 HMC03230
HUWE1 HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase 10075 300697 Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Pathological Conditions, Signs and Symptoms, Mental Disorders 7 CG8184 - FBgn0030674 CG8184 36714, 36715 HMS01604, HMS01605
TSFM Ts translation elongation factor, mitochondrial 10102 604723 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 8 CG6412 - FBgn0032646 CG6412 HMC03515
LRPPRC leucine-rich pentatricopeptide repeat containing 10128 607544 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 bsf bicoid stability factor FBgn0032679 CG10302 34550 HMS01022
AASS aminoadipate-semialdehyde synthase 10157 605113 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 LKR lysine ketoglutarate reductase FBgn0025687 CG7144 51850 HMC03424
ATP6AP2 ATPase, H+ transporting, lysosomal accessory protein 2 10159 300556 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 VhaM8.9 Vacuolar H[+] ATPase M8.9 accessory subunit FBgn0037671 CG8444
SLC25A15 solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 10166 603861 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG1628 - FBgn0030218 CG1628 54464 HMC03731
ALG3 asparagine-linked glycosylation 3, alpha-1,3- mannosyltransferase homolog (S. cerevisiae) 10195 608750 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 l(2)not lethal (2) neighbor of tid FBgn0011297 CG4084 53350 HMC03579
TOPORS topoisomerase I binding, arginine/serine-rich, E3 ubiquitin protein ligase 10210 609507 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7 Topors Topoisomerase I-interacting protein FBgn0267351 CG15104 34671 HMS01149
GPHN gephyrin 10243 603930 Musculoskeletal Diseases, Digestive System Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 cin cinnamon FBgn0000316 CG2945 32425, 53343 HMS00420, HMC03572, HMJ22231
ZMPSTE24 zinc metallopeptidase STE24 homolog (S. cerevisiae) 10269 606480 Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 ste24a prenyl protease type I FBgn0034176 CG9000 51880 HMC03454
EMG1 EMG1 nucleolar protein homolog (S. cerevisiae) 10436 611531 Musculoskeletal Diseases, Stomatognathic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7 CG3527 - FBgn0029714 CG3527
COG5 component of oligomeric golgi complex 5 10466 606821 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 fws four way stop FBgn0024689 CG6549 HMC04103
SEC23A Sec23 homolog A (S. cerevisiae) 10484 610511 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Male Urogenital Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Sec23 Sec23 ortholog (S. cerevisiae) FBgn0262125 CG1250 32365 HMS00356
NOP56 NOP56 ribonucleoprotein homolog (yeast) 10528 614154 Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 Nop56 Nop56 FBgn0038964 CG13849
RNASEH2A ribonuclease H2, subunit A 10535 606034 Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG13690 - FBgn0031252 CG13690 53326 HMC03555
SPTLC1 serine palmitoyltransferase, long chain base subunit 1 10558 605712 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 Spt-I Serine palmitoyltransferase subunit I FBgn0086532 CG4016 HMC03870
SLC19A2 solute carrier family 19 (thiamine transporter), member 2 10560 603941 Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 CG17036 - FBgn0032449 CG17036 51868 HMC03442
NPC2 Niemann-Pick disease, type C2 10577 601015 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Immune System Diseases, Mental Disorders 9 Npc2a Niemann-Pick type C-2a FBgn0031381 CG7291 38237 HMS01681
POMT1 protein-O-mannosyltransferase 1 10585 607423 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 rt rotated abdomen FBgn0003292 CG6097 51805 HMC03363
PRPF8 PRP8 pre-mRNA processing factor 8 homolog (S. cerevisiae) 10594 607300 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Prp8 pre-mRNA processing factor 8 FBgn0033688 CG8877 34622 HMS01297
PNPLA6 patatin-like phospholipase domain containing 6 10908 603197 Nervous System Diseases, Pathological Conditions, Signs and Symptoms 9 sws swiss cheese FBgn0003656 CG2212 HMC04094
AFG3L2 AFG3 ATPase family gene 3-like 2 (S. cerevisiae) 10939 604581 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG6512 - FBgn0036702 CG6512 34343 HMS01331
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4 10999 604194 Skin and Connective Tissue Diseases 10 Fatp Fatty acid (long chain) transport protein FBgn0267828 CG46149 50709 HMC03111, HMC03960, HMC04206
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4 10999 604194 Skin and Connective Tissue Diseases 10 CG44252 - FBgn0265187 CG44252 44658 HMC03958, HMC02440, HMJ22037
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4 10999 604194 Skin and Connective Tissue Diseases 10 CG44253 - FBgn0265188 CG44253 44658 HMC02440, HMJ22037
LIAS lipoic acid synthetase 11019 607031 Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 Las Lipoic acid synthase FBgn0029158 CG5231 HMC04106
SNRNP200 small nuclear ribonucleoprotein 200kDa (U5) 23020 601664 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 l(3)72Ab lethal (3) 72Ab FBgn0263599 CG5931 50716, 34024 HMS00994, HMS02950
ARHGAP26 Rho GTPase activating protein 26 23092 605370 Neoplasms 10 Graf GRAF ortholog (H. sapiens) FBgn0030685 CG8948 51853 HMC03427
SLC35D1 solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 23169 610804 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 frc fringe connection FBgn0042641 CG3874 42007 HMS02408
VPS13A vacuolar protein sorting 13 homolog A (S. cerevisiae) 23230 605978 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 9 Vps13 Vacuolar protein sorting 13 FBgn0033194 CG2093 38270, 42625 HMS01715, HMS02460
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific) 23236 607120 Nervous System Diseases 8 Plc21C Phospholipase C at 21C FBgn0004611 CG4574 32438, 33719 HMS00600, HMS00436
EHBP1 EH domain binding protein 1 23301 609922 Neoplasms, Male Urogenital Diseases 10 Ehbp1 Eps15 homology domain containing protein-binding protein 1 FBgn0034180 CG15609 42939 HMS02632
NCSTN nicastrin 23385 605254 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 nct nicastrin FBgn0039234 CG7012 57497 HMC04812
DICER1 dicer 1, ribonuclease type III 23405 606241 Neoplasms, Musculoskeletal Diseases, Respiratory Tract Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 9 Dcr-1 Dicer-1 FBgn0039016 CG4792 34826, 42901 HMS02594, HMS00141
SF3B1 splicing factor 3b, subunit 1, 155kDa 23451 605590 Hemic and Lymphatic Diseases 10 CG2807 - FBgn0031266 CG2807 33650 HMS00055
ETHE1 ethylmalonic encephalopathy 1 23474 608451 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG30022 - FBgn0050022 CG30022 53334 HMC03563
ISCU iron-sulfur cluster scaffold homolog (E. coli) 23479 611911 Musculoskeletal Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Nutritional and Metabolic Diseases 10 IscU IscU homolog FBgn0037637 CG9836 53277 HMC03493
SUZ12 suppressor of zeste 12 homolog (Drosophila) 23512 606245 Neoplasms, Female Urogenital Diseases and Pregnancy Complications 10 Su(z)12 Su(z)12 FBgn0020887 CG8013 33402 HMS00280
PIGN phosphatidylinositol glycan anchor biosynthesis, class N 23556 606097 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG2292 - FBgn0033479 CG2292 51875 HMC03449
PDSS1 prenyl (decaprenyl) diphosphate synthase, subunit 1 23590 607429 Musculoskeletal Diseases, Digestive System Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 qless qless FBgn0051005 CG31005
ORC6 origin recognition complex, subunit 6 23594 607213 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms 9 Orc6 Origin recognition complex subunit 6 FBgn0023180 CG1584
AMACR alpha-methylacyl-CoA racemase 23600 604489 Digestive System Diseases, Stomatognathic Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 CG9319 - FBgn0032881 CG9319 HMC03887
NUP62 nucleoporin 62kDa 23636 605815 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 Nup62 Nucleoporin 62kD FBgn0034118 CG6251 52927 HMC03668
FTSJ1 FtsJ RNA methyltransferase homolog 1 (E. coli) 24140 300499 Nervous System Diseases, Pathological Conditions, Signs and Symptoms 10 CG5220 - FBgn0038471 CG5220 53285 HMC03501
PRPF6 PRP6 pre-mRNA processing factor 6 homolog (S. cerevisiae) 24148 613979 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG6841 - FBgn0036828 CG6841 51909 HMC03484, HMC04384
RAB3GAP2 RAB3 GTPase activating protein subunit 2 (non-catalytic) 25782 609275 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 Rab3-GAP Rab3 GTPase activating protein FBgn0027505 CG7061 HMC04015
NIPBL Nipped-B homolog (Drosophila) 25836 608667 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 9 Nipped-B Nipped-B FBgn0026401 CG17704 32406 HMS00401
COG4 component of oligomeric golgi complex 4 25839 606976 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 CG7456 - FBgn0032258 CG7456 51866, 53679 HMC03440, HMJ21592, HMJ22023
NDUFAF3 NADH dehydrogenase (ubiquinone) complex I, assembly factor 3 25915 612911 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG5569 - FBgn0034919 CG5569 51894 HMC03468
CHMP2B charged multivesicular body protein 2B 25978 609512 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mental Disorders 10 CHMP2B Charged multivesicular body protein 2b FBgn0035589 CG4618 38375, 50942 HMJ21039, HMS01844
ABHD12 abhydrolase domain containing 12 26090 613599 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG15111 - FBgn0034419 CG15111 51885 HMC03459
PRPF31 PRP31 pre-mRNA processing factor 31 homolog (S. cerevisiae) 26121 606419 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Prp31 - FBgn0036487 CG6876 HMC04052
KIAA1279 KIAA1279 26128 609367 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG14043 - FBgn0031659 CG14043 51858 HMC03432
PHGDH phosphoglycerate dehydrogenase 26227 606879 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG6287 - FBgn0032350 CG6287 52928 HMC03669
B3GAT3 beta-1,3-glucuronyltransferase 3 (glucuronosyltransferase I) 26229 606374 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Cardiovascular Diseases, Skin and Connective Tissue Diseases 9 GlcAT-I GlcAT-I FBgn0066114 CG32775 34946 HMS00289
HIBCH 3-hydroxyisobutyryl-CoA hydrolase 26275 610690 Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 CG5044 - FBgn0038326 CG5044 52917 HMC03657
CHIC2 cysteine-rich hydrophobic domain 2 26511 604332 Neoplasms, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG5938 - FBgn0046247 CG5938 HMC03752
INTS6 integrator complex subunit 6 26512 604331 Neoplasms 8 IntS6 Integrator 6 FBgn0261383 CG3125 52904 HMC03644
TPK1 thiamin pyrophosphokinase 1 27010 606370 Musculoskeletal Diseases, Nervous System Diseases, Cardiovascular Diseases, Nutritional and Metabolic Diseases 9 CG14721 - FBgn0037942 CG14721
DNAI1 dynein, axonemal, intermediate chain 1 27019 604366 Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Immune System Diseases 9 CG9313 - FBgn0034566 CG9313 51888 HMC03462
ATP2C1 ATPase, Ca++ transporting, type 2C, member 1 27032 604384 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 SPoCk Secretory Pathway Calcium atpase FBgn0052451 CG32451 44040 HMS02756
B9D1 B9 protein domain 1 27077 614144 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 7 B9d1 B9d1 FBgn0038342 CG14870 52916 HMC03656
UQCRQ ubiquinol-cytochrome c reductase, complex III subunit VII, 9.5kDa 27089 612080 Musculoskeletal Diseases, Digestive System Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 10 UQCR-Q Ubiquinol-cytochrome c reductase ubiquinone-binding protein FBgn0036728 CG7580 51357 HMC03242
GNMT glycine N-methyltransferase 27232 606628 Digestive System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Gnmt Glycine N-methyltransferase FBgn0038074 CG6188 42637, 53282 HMC03498, HMS02473
COQ2 coenzyme Q2 homolog, prenyltransferase (yeast) 27235 609825 Musculoskeletal Diseases, Digestive System Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 Coq2 Coenzyme Q biosynthesis protein 2 FBgn0037574 CG9613 53276 HMC03492
NFU1 NFU1 iron-sulfur cluster scaffold homolog (S. cerevisiae) 27247 608100 Digestive System Diseases, Stomatognathic Diseases, Nutritional and Metabolic Diseases 6 CG33502 - FBgn0053502 CG33502 52907 HMC03647
HTRA2 HtrA serine peptidase 2 27429 606441 Nervous System Diseases 9 HtrA2 HTRA2-related serine protease FBgn0038233 CG8464 HMC03843
LAMTOR2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 28956 610389 Stomatognathic Diseases, Respiratory Tract Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 9 CG5189 - FBgn0034350 CG5189 51884, 38308 HMC03458, HMS01772
NDUFAF4 NADH dehydrogenase (ubiquinone) complex I, assembly factor 4 29078 611776 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG11722 - FBgn0037777 CG11722 52920 HMC03660
GPSM2 G-protein signaling modulator 2 29899 609245 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 8 pins partner of inscuteable FBgn0040080 CG5692 53968, 35048 HMS01462, HMJ21351
UBIAD1 UbiA prenyltransferase domain containing 1 29914 611632 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 heix heixuedian FBgn0028375 CG5876 51780 HMC03335
ALG6 asparagine-linked glycosylation 6, alpha-1,3-glucosyltransferase homolog (S. cerevisiae) 29929 604566 Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 gny garnysstan FBgn0032234 CG5091 51865 HMC03439
POMT2 protein-O-mannosyltransferase 2 29954 607439 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 tw Protein O-mannosyltransferase 2 FBgn0086368 CG12311 HMC03806
PSAT1 phosphoserine aminotransferase 1 29968 610936 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG11899 - FBgn0014427 CG11899 51476 HMC03221
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 50485 606622 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases, Immune System Diseases 9 Marcal1 Marcal1 FBgn0031655 CG3753 33709 HMS00587
DUOX2 dual oxidase 2 50506 606759 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 8 Duox Dual oxidase FBgn0031464 CG3131 33975, 32903 HMS00934, HMS00692
ASCC1 activating signal cointegrator 1 complex subunit 1 51008 614215 Neoplasms, Digestive System Diseases 9 CG12129 - FBgn0033475 CG12129 52889 HMC03627
WDPCP WD repeat containing planar cell polarity effector 51057 613580 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 frtz fritz FBgn0086698 CG17657 HMC03798
YARS2 tyrosyl-tRNA synthetase 2, mitochondrial 51067 610957 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases 10 Aats-tyr-m mitochondrial tyrosyl-tRNA synthetase FBgn0035064 CG16912 51895 HMC03469
NDUFAF1 NADH dehydrogenase (ubiquinone) complex I, assembly factor 1 51103 606934 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CIA30 Complex I intermediate-associated protein, 30 kDa FBgn0039689 CG7598 HMC03815
SBDS Shwachman-Bodian-Diamond syndrome 51119 607444 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG8549 - FBgn0035714 CG8549 54466, 58132 HMC03734, HMJ22081
SAR1B SAR1 homolog B (S. cerevisiae) 51128 607690 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Sar1 Sar1 ortholog (S. cerevisiae) FBgn0038947 CG7073 32364 HMS00355
DCXR dicarbonyl/L-xylulose reductase 51181 608347 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG7322 - FBgn0030968 CG7322 57152 HMC04529
CRBN cereblon 51185 609262 Nervous System Diseases, Pathological Conditions, Signs and Symptoms 8 CG3925 - FBgn0037780 CG3925 54467 HMC03735
GLRX5 glutaredoxin 5 51218 609588 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG14407 - FBgn0030584 CG14407
NT5C3 5'-nucleotidase, cytosolic III 51251 606224 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 cN-IIIB cytosolic 5'-nucleotidase IIIB FBgn0034988 CG3362 HMJ21695
KCNK9 potassium channel, subfamily K, member 9 51305 605874 Nervous System Diseases, Pathological Conditions, Signs and Symptoms, Mental Disorders 10 Task7 TWIK-related acid-sensitive K[+] channel 7 FBgn0037690 CG9361 53279 HMC03495
MBTPS2 membrane-bound transcription factor peptidase, site 2 51360 300294 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 S2P site-2 protease FBgn0033656 CG8988 35760 HMS01508, HMJ21986
TMEM138 transmembrane protein 138 51524 614459 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG13999 - FBgn0031753 CG13999 HMC03858
TRIM33 tripartite motif containing 33 51592 605769 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 7 bon bonus FBgn0023097 CG5206 37515 HMS01657
SUFU suppressor of fused homolog (Drosophila) 51684 607035 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Su(fu) Suppressor of fused FBgn0005355 CG6054 HMC04002
RAB23 RAB23, member RAS oncogene family 51715 606144 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases, Immune System Diseases 8 Rab23 Rab23 FBgn0037364 CG2108 HMC04039
UPB1 ureidopropionase, beta 51733 606673 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 pyd3 pyd3 FBgn0037513 CG3027 34557 HMS01029
WWOX WW domain containing oxidoreductase 51741 605131 Neoplasms, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Wwox WW domain containing oxidoreductase FBgn0031972 CG7221 44546, 51747 HMC03298, HMC02942
MYO3A myosin IIIA 53904 606808 Otorhinolaryngologic Diseases, Nervous System Diseases, Pathological Conditions, Signs and Symptoms 8 ninaC neither inactivation nor afterpotential C FBgn0002938 CG5125 HMC04022, HMC04132
GDAP1 ganglioside induced differentiation associated protein 1 54332 606598 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Gdap1 GDAP1 ortholog FBgn0035587 CG4623 51903 HMC03477
TMCO1 transmembrane and coiled-coil domains 1 54499 614123 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 10 CG10470 - FBgn0032746 CG10470 42896 HMS02589, HMC04195
PDP1 pyruvate dehyrogenase phosphatase catalytic subunit 1 54704 605993 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 Pdp Pyruvate dehydrogenase phosphatase FBgn0029958 CG12151 38972 HMS01888
DYM dymeclin 54808 607461 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG8230 - FBgn0027607 CG8230 HMC04016
CDKAL1 CDK5 regulatory subunit associated protein 1-like 1 54901 611259 Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 CG6550 - FBgn0034214 CG6550 51881 HMC03455
IMPAD1 inositol monophosphatase domain containing 1 54928 614010 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Skin and Connective Tissue Diseases 10 CG15743 - FBgn0030465 CG15743 51486 HMC03233
SDHAF2 succinate dehydrogenase complex assembly factor 2 54949 613019 Neoplasms, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 CG14757 - FBgn0033274 CG14757 54465 HMC03733
SDHAF2 succinate dehydrogenase complex assembly factor 2 54949 613019 Neoplasms, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 CG12895 - FBgn0033523 CG12895 51876 HMC03450
TMEM70 transmembrane protein 70 54968 612418 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 CG7506 - FBgn0035805 CG7506 53297 HMC03513
ATG16L1 autophagy related 16-like 1 (S. cerevisiae) 55054 610767 Digestive System Diseases 10 Atg16 Autophagy-related 16 FBgn0039705 CG31033 34358 HMS01347, HMJ22265
RBM28 RNA binding motif protein 28 55131 612074 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 CG4806 - FBgn0260456 CG4806
WRAP53 WD repeat containing, antisense to TP53 55135 612661 Stomatognathic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 WDR79 WD repeat domain 79 homolog FBgn0031782 CG9226 33363 HMS00235
MTPAP mitochondrial poly(A) polymerase 55149 613669 Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms 9 CG11418 - FBgn0024360 CG11418 52881 HMC03619
DARS2 aspartyl-tRNA synthetase 2, mitochondrial 55157 610956 Nervous System Diseases, Eye Diseases 9 CG31739 - FBgn0051739 CG31739 52909 HMC03649
PNPO pyridoxamine 5'-phosphate oxidase 55163 603287 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 sgll sugarlethal FBgn0051472 CG31472
SLC35C1 solute carrier family 35, member C1 55343 605881 Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 nac neuronally altered carbohydrate FBgn0265351 CG9620
NOP10 NOP10 ribonucleoprotein homolog (yeast) 55505 606471 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG7637 - FBgn0033548 CG7637 HMC03890
FOXRED1 FAD-dependent oxidoreductase domain containing 1 55572 613622 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 9 CG3270 - FBgn0033093 CG3270 52887 HMC03625
FLVCR2 feline leukemia virus subgroup C cellular receptor family, member 2 55640 610865 Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG1358 - FBgn0033196 CG1358
PIGV phosphatidylinositol glycan anchor biosynthesis, class V 55650 610274 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG44247 - FBgn0265182 CG44247 51478, 58114 HMC03223, HMJ22051
PIGV phosphatidylinositol glycan anchor biosynthesis, class V 55650 610274 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 veg vegetable FBgn0265195 - 51478, 58114 HMC03223, HMJ22051
NHP2 NHP2 ribonucleoprotein homolog (yeast) 55651 606470 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 NHP2 NHP2 FBgn0029148 CG5258 51784 HMC03339
TRMU tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase 55687 610230 Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Skin and Connective Tissue Diseases 10 CG3021 - FBgn0040337 CG3021 HMC03742
POLR3B polymerase (RNA) III (DNA directed) polypeptide B 55703 614366 Musculoskeletal Diseases, Digestive System Diseases, Respiratory Tract Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 RpIII128 RNA polymerase III 128kD subunit FBgn0004463 CG8344
VPS35 vacuolar protein sorting 35 homolog (S. cerevisiae) 55737 601501 Nervous System Diseases 9 Vps35 Vacuolar protein sorting 35 FBgn0034708 CG5625 38944 HMS01858
AGK acylglycerol kinase 55750 610345 Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 Mulk Multi-substrate lipid kinase FBgn0260750 CG31873 33046 HMS00699
IFT122 intraflagellar transport 122 homolog (Chlamydomonas) 55764 606045 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Oseg1 Outer segment 1 FBgn0265102 CG7161 51904 HMC03478
TDP1 tyrosyl-DNA phosphodiesterase 1 55775 607198 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 gkt glaikit FBgn0260817 CG8825
PSENEN presenilin enhancer 2 homolog (C. elegans) 55851 607632 Bacterial Infections and Mycoses, Skin and Connective Tissue Diseases 9 pen-2 presenilin enhancer FBgn0053198 CG33198 52908 HMC03648
ALG1 asparagine-linked glycosylation 1, beta-1,4-mannosyltransferase homolog (S. cerevisiae) 56052 605907 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 9 CG18012 - FBgn0038552 CG18012 53286 HMC03502
C10orf2 chromosome 10 open reading frame 2 56652 606075 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Endocrine System Diseases, Immune System Diseases, Mental Disorders 9 mtDNA-helicase mitochondrial DNA helicase FBgn0032154 CG5924
SMARCAD1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 56916 612761 Skin and Connective Tissue Diseases 8 Etl1 Etl1 homologue FBgn0032157 CG5899 33891 HMS00829
MCCC1 methylcrotonoyl-CoA carboxylase 1 (alpha) 56922 609010 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CG2118 - FBgn0039877 CG2118 38332, 40874 HMS02041, HMS01799
MRPS22 mitochondrial ribosomal protein S22 56945 605810 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 mRpS22 mitochondrial ribosomal protein S22 FBgn0039555 CG12261
COQ9 coenzyme Q9 homolog (S. cerevisiae) 57017 612837 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 CG30493 - FBgn0050493 CG30493 53336 HMC03565
RARS2 arginyl-tRNA synthetase 2, mitochondrial 57038 611524 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Skin and Connective Tissue Diseases 9 CG10092 - FBgn0037526 CG10092 53275, 58106 HMC03491, HMJ22021
PDSS2 prenyl (decaprenyl) diphosphate synthase, subunit 2 57107 610564 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 CG10585 - FBgn0037044 CG10585 51910, 43301 HMS02674, HMC03486
TBC1D24 TBC1 domain family, member 24 57465 613577 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 sky skywalker FBgn0032901 CG9339
WDR35 WD repeat domain 35 57539 613602 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Oseg4 Outer segment 4 FBgn0035264 CG2069 51898 HMC03472
IFT80 intraflagellar transport 80 homolog (Chlamydomonas) 57560 611177 Musculoskeletal Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 Oseg5 Outer segment 5 FBgn0032891 CG9333 HMC03888
WDR19 WD repeat domain 19 57728 608151 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases 10 Oseg6 Outer segment 6 FBgn0034452 CG11237 51887 HMC03461
SLC25A19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 60386 606521 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Tpc1 Thiamine pyrophosphate carrier protein 1 FBgn0037852 CG6608 HMJ21997
ELAC2 elaC homolog 2 (E. coli) 60528 605367 Neoplasms, Male Urogenital Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 JhI-1 Juvenile hormone-inducible protein 1 FBgn0028426 CG3298 51781 HMC03826, HMC03336
MCCC2 methylcrotonoyl-CoA carboxylase 2 (beta) 64087 609014 Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 CG3267 - FBgn0042083 CG3267 52912 HMC03652
XYLT1 xylosyltransferase I 64131 608124 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 oxt peptide O-xylosyltransferase FBgn0015360 CG32300 38985 HMS01901, HMC02377
XYLT2 xylosyltransferase II 64132 608125 Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 oxt peptide O-xylosyltransferase FBgn0015360 CG32300 38985 HMS01901, HMC02377
SIL1 SIL1 homolog, endoplasmic reticulum chaperone (S. cerevisiae) 64374 608005 Musculoskeletal Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 9 CG10420 - FBgn0039296 CG10420 33968 HMS00925
RBM15 RNA binding motif protein 15 64783 606077 Neoplasms 9 nito spenito FBgn0027548 CG2910 34848 HMS00166, HMJ02081, HMS02013
PORCN porcupine homolog (Drosophila) 64840 300651 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 por porcupine FBgn0004957 CG6205 57380 HMC04684
UPF3B UPF3 regulator of nonsense transcripts homolog B (yeast) 65109 300298 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Mental Disorders 9 Upf3 Upf3 FBgn0034923 CG11184 44565, 58181 HMS02861, HMJ22158
PCDH15 protocadherin-related 15 65217 605514 Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Cad99C Cadherin 99C FBgn0039709 CG31009 35037 HMS01451
VKORC1 vitamin K epoxide reductase complex, subunit 1 79001 608547 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 Vkor Vitamin-K epoxide reductase FBgn0053544 CG33544
ALG8 asparagine-linked glycosylation 8, alpha-1,3-glucosyltransferase homolog (S. cerevisiae) 79053 608103 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 xit xiantuan FBgn0029906 CG4542 HMC03884
ASPSCR1 alveolar soft part sarcoma chromosome region, candidate 1 79058 606236 Neoplasms 8 CG33722 - FBgn0064126 CG33722
ALG12 asparagine-linked glycosylation 12, alpha-1,6-mannosyltransferase homolog (S. cerevisiae) 79087 607144 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG8412 - FBgn0037743 CG8412 34680 HMS01158
C20orf7 NADH dehydrogenase (ubiquinone) complex I, assembly factor 5 79133 612360 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG8067 - FBgn0033891 CG8067 51879 HMC03453
FKRP fukutin related protein 79147 606596 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG15651 - FBgn0034567 CG15651 51889 HMC03463
TMEM43 transmembrane protein 43 79188 612048 Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG8111 - FBgn0035825 CG8111
CDC73 cell division cycle 73, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae) 79577 607393 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases 10 hyx hyrax FBgn0037657 CG11990 53278 HMC03494
RNASEH2B ribonuclease H2, subunit B 79621 610326 Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG11164 - FBgn0030507 CG11164
SRD5A3 steroid 5 alpha-reductase 3 79644 611715 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 10 CG7840 - FBgn0032014 CG7840 32379, 34954 HMS00370, HMS00426
C16orf57 chromosome 16 open reading frame 57 79650 613276 Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Skin and Connective Tissue Diseases, Immune System Diseases 10 CG16790 - FBgn0037713 CG16790
SLC25A22 solute carrier family 25 (mitochondrial carrier: glutamate), member 22 79751 609302 Musculoskeletal Diseases, Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 GC1 Glutamate Carrier 1 FBgn0260743 CG18347 34890 HMS01235
C7orf10 chromosome 7 open reading frame 10 79783 609187 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CG10877 - FBgn0038804 CG10877 HMC03835
L2HGDH L-2-hydroxyglutarate dehydrogenase 79944 609584 Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG10639 - FBgn0032729 CG10639 51870 HMC03444
DHDDS dehydrodolichyl diphosphate synthase 79947 608172 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 CG10778 - FBgn0029980 CG10778 51815 HMC03386
BICC1 bicaudal C homolog 1 (Drosophila) 80114 614295 Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases 10 BicC Bicaudal C FBgn0000182 CG4824 34997 HMS01407
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) 80207 606580 Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG13601 - FBgn0039126 CG13601
NUBPL nucleotide binding protein-like 80224 613621 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 CG3262 - FBgn0032986 CG3262 51873 HMC03447
PUS1 pseudouridylate synthase 1 80324 608109 Musculoskeletal Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 10 CG4159 - FBgn0038811 CG4159 53288 HMC03504
CDT1 chromatin licensing and DNA replication factor 1 81620 605525 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Pathological Conditions, Signs and Symptoms 9 dup double parked FBgn0000996 CG8171
VANGL1 vang-like 1 (van gogh, Drosophila) 81839 610132 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Vang Van Gogh FBgn0015838 CG8075 34354 HMS01343
SBF2 SET binding factor 2 81846 607697 Musculoskeletal Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 Sbf SET domain binding factor FBgn0025802 CG6939 44004, 32419, 57301 HMS02718, HMS00414, HMS04499
MED25 mediator complex subunit 25 81857 610197 Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 MED25 Mediator complex subunit 25 FBgn0038760 CG12254 33595, 42501 HMS00256, HMJ02066
DNAL1 dynein, axonemal, light chain 1 83544 610062 Musculoskeletal Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases 10 CG8800 - FBgn0033408 CG8800 53295 HMC03511
C19orf12 chromosome 19 open reading frame 12 83636 614297 Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Skin and Connective Tissue Diseases 10 CG3740 - FBgn0023530 CG3740 HMC02677
TRAPPC9 trafficking protein particle complex 9 83696 611966 Nervous System Diseases, Pathological Conditions, Signs and Symptoms, Mental Disorders 9 bru brunelleschi FBgn0261787 CG2478
ARL6 ADP-ribosylation factor-like 6 84100 608845 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Arl6 ADP ribosylation factor-like 6 FBgn0034446 CG7735 51886 HMC03460
COG8 component of oligomeric golgi complex 8 84342 606979 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG6488 - FBgn0032361 CG6488 HMC03886
LMNB2 lamin B2 84823 150341 Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 LamC Lamin C FBgn0010397 CG10119
ORAI1 ORAI calcium release-activated calcium modulator 1 84876 610277 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Immune System Diseases 10 olf186-F olf186-F FBgn0041585 CG11430 53333 HMC03562
CIRH1A cirrhosis, autosomal recessive 1A (cirhin) 84916 607456 Pathological Conditions, Signs and Symptoms 10 l(3)72Dn lethal (3) 72Dn FBgn0263605 CG5018 51907 HMC03482
ALG10 asparagine-linked glycosylation 10, alpha-1,2-glucosyltransferase homolog (S. pombe) 84920 603313 Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Alg10 Alpha 3 glucosyltransferase FBgn0052076 CG32076 34681 HMS01159
MASTL microtubule associated serine/threonine kinase-like 84930 608221 Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 9 gwl greatwall FBgn0260399 CG7719 34525 HMS00834
ALG2 asparagine-linked glycosylation 2, alpha-1,3-mannosyltransferase homolog (S. cerevisiae) 85365 607905 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG1291 - FBgn0035401 CG1291 HMC03827, HMJ21645
GFM1 G elongation factor, mitochondrial 1 85476 606639 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 10 ico iconoclast FBgn0263133 CG4567
TMEM67 transmembrane protein 67 91147 609884 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Endocrine System Diseases, Immune System Diseases 9 CG15923 - FBgn0038814 CG15923 53289 HMC03505
SLC39A13 solute carrier family 39 (zinc transporter), member 13 91252 608735 Musculoskeletal Diseases, Stomatognathic Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 Zip99C Zinc/iron regulated transporter-related protein 99C FBgn0039714 CG7816 50635 HMC03033
C12orf65 chromosome 12 open reading frame 65 91574 613541 Digestive System Diseases, Stomatognathic Diseases, Eye Diseases, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 CG30100 - FBgn0050100 CG30100 53335 HMC03564
ATPAF2 ATP synthase mitochondrial F1 complex assembly factor 2 91647 608918 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases 9 l(2)k14505 lethal (2) k14505 FBgn0021856 CG8674 53352 HMC03581
RFT1 RFT1 homolog (S. cerevisiae) 91869 611908 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG3149 - FBgn0027564 CG3149 53324 HMC03553
COG7 component of oligomeric golgi complex 7 91949 606978 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 10 Cog7 Cog7 FBgn0051040 CG31040 HMC03758
STRADA STE20-related kinase adaptor alpha 92335 608626 Female Urogenital Diseases and Pregnancy Complications 9 Stlk Ste20-like kinase FBgn0046692 CG40293 34620 HMS01295
PIGM phosphatidylinositol glycan anchor biosynthesis, class M 93183 610273 Digestive System Diseases, Nervous System Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Immune System Diseases 9 CG9865 - FBgn0034649 CG9865 38321, 51890 HMS01785, HMC03464
C20orf54 solute carrier family 52, riboflavin transporter, member 3 113278 613350 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG11576 - FBgn0039882 CG11576 57498 HMC04813
RXFP2 relaxin/insulin-like family peptide receptor 2 122042 606655 Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications 10 Lgr3 Leucine-rich repeat-containing G protein-coupled receptor 3 FBgn0039354 CG31096 HMC04196
TTC8 tetratricopeptide repeat domain 8 123016 608132 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 BBS8 Bardet-Biedl syndrome 8 ortholog (H. sapiens) FBgn0031255 CG13691
CANT1 calcium activated nucleotidase 1 124583 613165 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG5276 - FBgn0037900 CG5276 52918 HMC03658
USH1G Usher syndrome 1G (autosomal recessive) 124590 607696 Otorhinolaryngologic Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 Sans Sans ortholog FBgn0033785 CG13320 52890 HMC03628
GIPC3 GIPC PDZ domain containing family, member 3 126326 608792 Otorhinolaryngologic Diseases, Nervous System Diseases, Pathological Conditions, Signs and Symptoms 9 kermit kermit FBgn0010504 CG11546 53349 HMC03578
CHMP4B charged multivesicular body protein 4B 128866 610897 Eye Diseases 10 shrb shrub FBgn0086656 CG8055 38305 HMS01767
GLYCTK glycerate kinase 132158 610516 Musculoskeletal Diseases, Nutritional and Metabolic Diseases 10 CG9886 - FBgn0031428 CG9886 51857 HMC03431
WDR36 WD repeat domain 36 134430 609669 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9 CG9799 - FBgn0038146 CG9799
C8orf38 NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 137682 612392 Musculoskeletal Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Nutritional and Metabolic Diseases, Mental Disorders 9 sicily severe impairment of CI with lengthened youth FBgn0030352 CG15738 HMC04019
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase 138050 610453 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Immune System Diseases, Mental Disorders 9 CG6903 - FBgn0029737 CG6903 33423 HMS00307
B3GALTL beta 1,3-galactosyltransferase-like 145173 610308 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 CG9109 - FBgn0031765 CG9109
VPS13B vacuolar protein sorting 13 homolog B (yeast) 157680 607817 Musculoskeletal Diseases, Stomatognathic Diseases, Otorhinolaryngologic Diseases, Nervous System Diseases, Eye Diseases, Cardiovascular Diseases, Hemic and Lymphatic Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Endocrine System Diseases 9 CG15523 - FBgn0039727 CG15523 52915 HMC03655
BMPER BMP binding endothelial regulator 168667 608699 Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Otorhinolaryngologic Diseases, Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 8 cv-2 crossveinless 2 FBgn0000395 CG15671 37514 HMS01656
ACSF3 acyl-CoA synthetase family member 3 197322 614245 Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases 9 CG18155 - FBgn0029945 CG18155 52884 HMC03622
PIKFYVE phosphoinositide kinase, FYVE finger containing 200576 609414 Eye Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8 fab1 - FBgn0028741 CG6355 51782 HMC03337
FLCN folliculin 201163 607273 Neoplasms, Musculoskeletal Diseases, Digestive System Diseases, Stomatognathic Diseases, Respiratory Tract Diseases, Male Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases 10 BHD Birt-Hogg-Dube homolog FBgn0261111 CG8616


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