Protein List

Listed below are all the proteins used in our analysis. You can refine the list by using the panel below.
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UniProtID Disease Name

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Found 257  pleiotropic proteins  (16.0 %) and 1345 non-pleiotropic proteins (84.0 %).


1602 items found (page 1 of 33)

Gene UniProt Protein Type Disease
AAAS Q9NRG9 non-pleiotropic Achalasia-addisonianism-alacrima syndrome (AAAS) [MIM:231550]
AANAT Q16613 non-pleiotropic Delayed sleep phase syndrome (DSPS) [MIM:614163]
AARS P49588 non-pleiotropic Charcot-Marie-Tooth disease 2N (CMT2N) [MIM:613287]
AARS2 Q5JTZ9 non-pleiotropic Combined oxidative phosphorylation deficiency 8 (COXPD8) [MIM:614096]
ABAT P80404 non-pleiotropic GABA transaminase deficiency (GABATD) [MIM:613163]
ABCA3 Q99758 non-pleiotropic Pulmonary surfactant metabolism dysfunction 3 (SMDP3) [MIM:610921]
ABCB4 P21439 pleiotropic Cholestasis of pregnancy, intrahepatic 3 (ICP3) [MIM:614972]
Gallbladder disease 1 (GBD1) [MIM:600803]
Cholestasis, progressive familial intrahepatic, 3 (PFIC3) [MIM:602347]
ABCB7 O75027 non-pleiotropic Anemia, sideroblastic, spinocerebellar ataxia (ASAT) [MIM:301310]
ABCC2 Q92887 non-pleiotropic Dubin-Johnson syndrome (DJS) [MIM:237500]
ABCC6 O95255 pleiotropic Pseudoxanthoma elasticum (PXE) [MIM:264800]
Arterial calcification of infancy, generalized, 2 (GACI2) [MIM:614473]
ABCC8 Q09428 pleiotropic Familial hyperinsulinemic hypoglycemia 1 (HHF1) [MIM:256450]
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176]
Transient neonatal diabetes mellitus 2 (TNDM2) [MIM:610374]
Leucine-induced hypoglycemia (LIH) [MIM:240800]
ABCC9 O60706 pleiotropic Cardiomyopathy, dilated 1O (CMD1O) [MIM:608569]
Atrial fibrillation, familial, 12 (ATFB12) [MIM:614050]
Hypertrichotic osteochondrodysplasia (HTOCD) [MIM:239850]
ABCD4 O14678 non-pleiotropic Methylmalonic aciduria and homocystinuria type cblJ (MAHCJ) [MIM:614857]
ABCG5 Q9H222 non-pleiotropic Sitosterolemia (STSL) [MIM:210250]
ABHD5 Q8WTS1 non-pleiotropic Chanarin-Dorfman syndrome (CDS) [MIM:275630]
ACAD8 Q9UKU7 non-pleiotropic Isobutyryl-CoA dehydrogenase deficiency (IBDD) [MIM:611283]
ACADM P11310 non-pleiotropic Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450]
ACADS P16219 non-pleiotropic Acyl-CoA dehydrogenase short-chain deficiency (ACADSD) [MIM:201470]
ACADSB P45954 non-pleiotropic Short/branched-chain acyl-CoA dehydrogenase deficiency (SBCADD) [MIM:610006]
ACADVL P49748 non-pleiotropic Acyl-CoA dehydrogenase very long-chain deficiency (ACADVLD) [MIM:201475]
ACAN P16112 pleiotropic Spondyloepimetaphyseal dysplasia aggrecan type (SEMD-ACAN) [MIM:612813]
Osteochondritis dissecans short stature and early-onset osteoarthritis (OD) [MIM:165800]
ACAT1 P24752 non-pleiotropic 3-ketothiolase deficiency (3KTD) [MIM:203750]
ACO2 Q99798 non-pleiotropic Infantile cerebellar-retinal degeneration (ICRD) [MIM:614559]
ACOX1 Q15067 non-pleiotropic Adrenoleukodystrophy, pseudoneonatal (Pseudo-NALD) [MIM:264470]
ACP5 P13686 non-pleiotropic Spondyloenchondrodysplasia with immune dysregulation (SPENCDI) [MIM:607944]
ACSF3 Q4G176 non-pleiotropic Combined malonic and methylmalonic aciduria (CMAMMA) [MIM:614265]
ACSL4 O60488 non-pleiotropic Mental retardation, X-linked 63 (MRX63) [MIM:300387]
ACTA2 P62736 pleiotropic Aortic aneurysm, familial thoracic 6 (AAT6) [MIM:611788]
Moyamoya disease 5 (MYMY5) [MIM:614042]
Multisystemic smooth muscle dysfunction syndrome (MSMDYS) [MIM:613834]
ACTB P60709 pleiotropic Dystonia, juvenile-onset (DYTJ) [MIM:607371]
Baraitser-Winter syndrome 1 (BRWS1) [MIM:243310]
ACTC1 P68032 pleiotropic Cardiomyopathy, familial hypertrophic 11 (CMH11) [MIM:612098]
Cardiomyopathy, dilated 1R (CMD1R) [MIM:613424]
Atrial septal defect 5 (ASD5) [MIM:612794]
ACTG1 P63261 pleiotropic Deafness, autosomal dominant, 20 (DFNA20) [MIM:604717]
Baraitser-Winter syndrome 2 (BRWS2) [MIM:614583]
ACTN1 P12814 non-pleiotropic Bleeding disorder, platelet-type 15 (BDPLT15) [MIM:615193]
ACTN2 P35609 non-pleiotropic Cardiomyopathy, dilated 1AA (CMD1AA) [MIM:612158]
ACTN4 O43707 non-pleiotropic Focal segmental glomerulosclerosis 1 (FSGS1) [MIM:603278]
ACVR1 Q04771 non-pleiotropic Fibrodysplasia ossificans progressiva (FOP) [MIM:135100]
ACVR2B Q13705 non-pleiotropic Heterotaxy, visceral, 4, autosomal (HTX4) [MIM:613751]
ACVRL1 P37023 non-pleiotropic Telangiectasia, hereditary hemorrhagic, 2 (HHT2) [MIM:600376]
ACY1 Q03154 non-pleiotropic Aminoacylase-1 deficiency (ACY1D) [MIM:609924]
ADAMTS10 Q9H324 non-pleiotropic Weill-Marchesani syndrome 1 (WMS1) [MIM:277600]
ADAMTS13 Q76LX8 non-pleiotropic Thrombotic thrombocytopenic purpura congenital (TTP) [MIM:274150]
ADAMTS18 Q8TE60 non-pleiotropic Microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) [MIM:615458]
ADAMTSL2 Q86TH1 non-pleiotropic Geleophysic dysplasia 1 (GPHYSD1) [MIM:231050]
ADAR P55265 pleiotropic Dyschromatosis symmetrica hereditaria (DSH) [MIM:127400]
Aicardi-Goutieres syndrome 6 (AGS6) [MIM:615010]
ADAT3 Q96EY9 non-pleiotropic Mental retardation, autosomal recessive 36 (MRT36) [MIM:615286]
ADCK3 Q8NI60 non-pleiotropic Coenzyme Q10 deficiency, primary, 4 (COQ10D4) [MIM:612016]
ADCK4 Q96D53 non-pleiotropic Nephrotic syndrome 9 (NPHS9) [MIM:615573]
ADCY5 O95622 non-pleiotropic Dyskinesia, familial, with facial myokymia (FDFM) [MIM:606703]
ADIPOQ Q15848 non-pleiotropic Adiponectin deficiency (ADPND) [MIM:612556]
ADK P55263 non-pleiotropic Hypermethioninemia due to adenosine kinase deficiency (HMAKD) [MIM:614300]
ADSL P30566 non-pleiotropic Adenylosuccinase deficiency (ADSL deficiency) [MIM:103050]