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 23 of 33)

Gene UniProt Protein Type Disease
PLCD1 P51178 non-pleiotropic Nail disorder, non-syndromic congenital, 3 (NDNC3) [MIM:151600]
PLCE1 Q9P212 non-pleiotropic Nephrotic syndrome 3 (NPHS3) [MIM:610725]
PLEC Q15149 non-pleiotropic Epidermolysis bullosa simplex, Ogna type (O-EBS) [MIM:131950]
PLG P00747 non-pleiotropic Plasminogen deficiency (PLGD) [MIM:217090]
PLOD1 Q02809 non-pleiotropic Ehlers-Danlos syndrome 6 (EDS6) [MIM:225400]
PLOD2 O00469 non-pleiotropic Bruck syndrome 2 (BRKS2) [MIM:609220]
PLOD3 O60568 non-pleiotropic Lysyl hydroxylase 3 deficiency (LH3 deficiency) [MIM:612394]
PLP1 P60201 pleiotropic Leukodystrophy, hypomyelinating, 1 (HLD1) [MIM:312080]
Spastic paraplegia 2, X-linked (SPG2) [MIM:312920]
PMM2 O15305 non-pleiotropic Congenital disorder of glycosylation 1A (CDG1A) [MIM:212065]
PNKD Q8N490 non-pleiotropic Dystonia 8 (DYT8) [MIM:118800]
PNKP Q96T60 non-pleiotropic Epileptic encephalopathy, early infantile, 10 (EIEE10) [MIM:613402]
PNP P00491 non-pleiotropic Purine nucleoside phosphorylase deficiency (PNPD) [MIM:613179]
PNPLA1 Q8N8W4 non-pleiotropic Ichthyosis, congenital, autosomal recessive 10 (ARCI10) [MIM:615024]
PNPLA2 Q96AD5 non-pleiotropic Neutral lipid storage disease with myopathy (NLSDM) [MIM:610717]
PNPO Q9NVS9 non-pleiotropic Pyridoxine-5'-phosphate oxidase deficiency (PNPO deficiency) [MIM:610090]
POC1A Q8NBT0 non-pleiotropic Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis (SOFT) [MIM:614813]
POF1B Q8WVV4 non-pleiotropic Premature ovarian failure 2B (POF2B) [MIM:300604]
POLD1 P28340 non-pleiotropic Colorectal cancer 10 (CRCS10) [MIM:612591]
POLE Q07864 non-pleiotropic Colorectal cancer 12 (CRCS12) [MIM:615083]
POLG P54098 pleiotropic Progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal recessive (PEOB) [MIM:258450]
Mitochondrial DNA depletion syndrome 4A (MTDPS4A) [MIM:203700]
Sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO) [MIM:607459]
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 1 (PEOA1) [MIM:157640]
Mitochondrial DNA depletion syndrome 4B (MTDPS4B) [MIM:613662]
Leigh syndrome (LS) [MIM:256000]
POLG2 Q9UHN1 non-pleiotropic Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 4 (PEOA4) [MIM:610131]
POLH Q9Y253 non-pleiotropic Xeroderma pigmentosum variant type (XPV) [MIM:278750]
POLR1C O15160 non-pleiotropic Treacher Collins syndrome 3 (TCS3) [MIM:248390]
POLR1D Q9Y2S0 non-pleiotropic Treacher Collins syndrome 2 (TCS2) [MIM:613717]
POLR3A O14802 non-pleiotropic Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism (HLD7) [MIM:607694]
POLR3B Q9NW08 non-pleiotropic Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism (HLD8) [MIM:614381]
POMGNT2 Q8NAT1 non-pleiotropic Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A8 (MDDGA8) [MIM:614830]
POMK Q9H5K3 non-pleiotropic Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A12 (MDDGA12) [MIM:615249]
PORCN Q9H237 non-pleiotropic Focal dermal hypoplasia (FODH) [MIM:305600]
POU1F1 P28069 non-pleiotropic Pituitary hormone deficiency, combined, 1 (CPHD1) [MIM:613038]
POU3F4 P49335 non-pleiotropic Deafness, X-linked, 2 (DFNX2) [MIM:304400]
POU4F3 Q15319 non-pleiotropic Deafness, autosomal dominant, 15 (DFNA15) [MIM:602459]
POU6F2 P78424 non-pleiotropic Hereditary susceptibility to Wilms tumor 5 (WT5) [MIM:601583]
PPARG P37231 pleiotropic Obesity (OBESITY) [MIM:601665]
Lipodystrophy, familial partial, 3 (FPLD3) [MIM:604367]
PPIB P23284 non-pleiotropic Osteogenesis imperfecta 9 (OI9) [MIM:259440]
PPOX P50336 non-pleiotropic Variegate porphyria (VP) [MIM:176200]
PPP1R3A Q16821 non-pleiotropic Diabetes mellitus, non-insulin-dependent (NIDDM) [MIM:125853]
PPT1 P50897 non-pleiotropic Ceroid lipofuscinosis, neuronal, 1 (CLN1) [MIM:256730]
PQBP1 O60828 non-pleiotropic Renpenning syndrome 1 (RENS1) [MIM:309500]
PRCD Q00LT1 non-pleiotropic Retinitis pigmentosa 36 (RP36) [MIM:610599]
PRDM16 Q9HAZ2 non-pleiotropic Cardiomyopathy, dilated 1LL (CMD1LL) [MIM:615373]
Left ventricular non-compaction 8 (LVNC8) [MIM:615373]
PRDM5 Q9NQX1 non-pleiotropic Brittle cornea syndrome 2 (BCS2) [MIM:614170]
PRICKLE1 Q96MT3 non-pleiotropic Epilepsy, progressive myoclonic 1B (EPM1B) [MIM:612437]
PRICKLE2 Q7Z3G6 non-pleiotropic Epilepsy, progressive myoclonic 5 (EPM5) [MIM:613832]
PRIMPOL Q96LW4 non-pleiotropic Myopia 22, autosomal dominant (MYP22) [MIM:615420]
PRKAR1A P10644 pleiotropic Carney complex 1 (CNC1) [MIM:160980]
Acrodysostosis 1, with or without hormone resistance (ACRDYS1) [MIM:101800]
PRKCG P05129 non-pleiotropic Spinocerebellar ataxia 14 (SCA14) [MIM:605361]
PRKG1 Q13976 non-pleiotropic Aortic aneurysm, familial thoracic 8 (AAT8) [MIM:615436]
PRKRA O75569 non-pleiotropic Dystonia 16 (DYT16) [MIM:612067]
PROK2 Q9HC23 non-pleiotropic Hypogonadotropic hypogonadism 4 with or without anosmia (HH4) [MIM:610628]