Found 257 pleiotropic proteins (16.0 %) and 1345 non-pleiotropic proteins (84.0 %).
1602 items found (page 3 of 33)
Gene | UniProt | Protein Type | Disease |
---|---|---|---|
ANKS6 | Q68DC2 | non-pleiotropic | Nephronophthisis 16 (NPHP16) [MIM:615382] |
ANO10 | Q9NW15 | non-pleiotropic | Spinocerebellar ataxia, autosomal recessive, 10 (SCAR10) [MIM:613728] |
ANO3 | Q9BYT9 | non-pleiotropic | Dystonia 24 (DYT24) [MIM:615034] |
ANTXR2 | P58335 | non-pleiotropic | Hyaline fibromatosis syndrome (HFS) [MIM:228600] |
AP2S1 | P53680 | non-pleiotropic | Hypocalciuric hypercalcemia, familial 3 (HHC3) [MIM:600740] |
AP3B1 | O00203 | non-pleiotropic | Hermansky-Pudlak syndrome 2 (HPS2) [MIM:608233] |
APC | P25054 | pleiotropic | Familial adenomatous polyposis (FAP) [MIM:175100] Gastric cancer (GASC) [MIM:613659] Medulloblastoma (MDB) [MIM:155255] |
APCDD1 | Q8J025 | non-pleiotropic | Hypotrichosis 1 (HYPT1) [MIM:605389] |
APOC2 | P02655 | non-pleiotropic | Hyperlipoproteinemia 1B (HLPP1B) [MIM:207750] |
APOC3 | P02656 | non-pleiotropic | Hyperalphalipoproteinemia 2 (HALP2) [MIM:614028] |
APP | P05067 | pleiotropic | Alzheimer disease 1 (AD1) [MIM:104300] Cerebral amyloid angiopathy, APP-related (CAA-APP) [MIM:605714] |
APRT | P07741 | non-pleiotropic | Adenine phosphoribosyltransferase deficiency (APRTD) [MIM:614723] |
APTX | Q7Z2E3 | non-pleiotropic | Ataxia-oculomotor apraxia syndrome (AOA) [MIM:208920] |
AQP2 | P41181 | non-pleiotropic | Diabetes insipidus, nephrogenic, autosomal (ANDI) [MIM:125800] |
AQP5 | P55064 | non-pleiotropic | Keratoderma, palmoplantar, Bothnian type (PPKB) [MIM:600231] |
ARFGEF2 | Q9Y6D5 | non-pleiotropic | Periventricular nodular heterotopia 2 (PVNH2) [MIM:608097] |
ARG1 | P05089 | non-pleiotropic | Argininemia (ARGIN) [MIM:207800] |
ARHGAP26 | Q9UNA1 | non-pleiotropic | Leukemia, juvenile myelomonocytic (JMML) [MIM:607785] |
ARHGEF10 | O15013 | non-pleiotropic | Slowed nerve conduction velocity (SNCV) [MIM:608236] |
ARHGEF9 | O43307 | non-pleiotropic | Epileptic encephalopathy, early infantile, 8 (EIEE8) [MIM:300607] |
ARL13B | Q3SXY8 | non-pleiotropic | Joubert syndrome 8 (JBTS8) [MIM:612291] |
ARL2BP | Q9Y2Y0 | non-pleiotropic | Retinitis pigmentosa with or without situs inversus (RPSI) [MIM:615434] |
ARL6 | Q9H0F7 | pleiotropic | Bardet-Biedl syndrome 3 (BBS3) [MIM:209900] Retinitis pigmentosa 55 (RP55) [MIM:613575] |
ARMC4 | Q5T2S8 | non-pleiotropic | Ciliary dyskinesia, primary, 23 (CILD23) [MIM:615451] |
ARSA | P15289 | non-pleiotropic | Leukodystrophy metachromatic (MLD) [MIM:250100] |
ARSB | P15848 | non-pleiotropic | Mucopolysaccharidosis 6 (MPS6) [MIM:253200] |
ARSE | P51690 | non-pleiotropic | Chondrodysplasia punctata 1, X-linked recessive (CDPX1) [MIM:302950] |
ARX | Q96QS3 | pleiotropic | Lissencephaly, X-linked 2 (LISX2) [MIM:300215] Epileptic encephalopathy, early infantile, 1 (EIEE1) [MIM:308350] Mental retardation, X-linked, ARX-related (MRXARX) [MIM:300419] Agenesis of the corpus callosum, with abnormal genitalia (ACCAG) [MIM:300004] |
ASAH1 | Q13510 | pleiotropic | Farber lipogranulomatosis (FL) [MIM:228000] Spinal muscular atrophy with progressive myoclonic epilepsy (SMAPME) [MIM:159950] |
ASL | P04424 | non-pleiotropic | Argininosuccinic aciduria (ARGINSA) [MIM:207900] |
ASNS | P08243 | non-pleiotropic | Asparagine synthetase deficiency (ASNSD) [MIM:615574] |
ASPA | P45381 | non-pleiotropic | Canavan disease (CAND) [MIM:271900] |
ASS1 | P00966 | non-pleiotropic | Citrullinemia 1 (CTLN1) [MIM:215700] |
ATCAY | Q86WG3 | non-pleiotropic | Cerebellar ataxia, cayman type (ATCAY) [MIM:601238] |
ATIC | P31939 | non-pleiotropic | AICAR transformylase/IMP cyclohydrolase deficiency (AICAR) [MIM:608688] |
ATL1 | Q8WXF7 | pleiotropic | Spastic paraplegia 3, autosomal dominant (SPG3) [MIM:182600] Neuropathy, hereditary sensory, 1D (HSN1D) [MIM:613708] |
ATL3 | Q6DD88 | non-pleiotropic | Neuropathy, hereditary sensory, 1F (HSN1F) [MIM:615632] |
ATP13A2 | Q9NQ11 | non-pleiotropic | Kufor-Rakeb syndrome (KRS) [MIM:606693] Ceroid lipofuscinosis, neuronal, 12 (CLN12) [MIM:606693] |
ATP1A2 | P50993 | pleiotropic | Alternating hemiplegia of childhood 1 (AHC1) [MIM:104290] Migraine, familial hemiplegic, 2 (FHM2) [MIM:602481] |
ATP1A3 | P13637 | pleiotropic | Dystonia 12 (DYT12) [MIM:128235] Alternating hemiplegia of childhood 2 (AHC2) [MIM:614820] |
ATP2A1 | O14983 | non-pleiotropic | Brody myopathy (BRM) [MIM:601003] |
ATP2B3 | Q16720 | non-pleiotropic | Spinocerebellar ataxia, X-linked 1 (SCAX1) [MIM:302500] |
ATP2C1 | P98194 | non-pleiotropic | Hailey-Hailey disease (HHD) [MIM:169600] |
ATP5A1 | P25705 | non-pleiotropic | Mitochondrial complex V deficiency, nuclear 4 (MC5DN4) [MIM:615228] |
ATP5E | P56381 | non-pleiotropic | Mitochondrial complex V deficiency, nuclear 3 (MC5DN3) [MIM:614053] |
ATP6V0A4 | Q9HBG4 | non-pleiotropic | Renal tubular acidosis, distal, autosomal recessive (RTADR) [MIM:602722] |
ATP6V1B1 | P15313 | non-pleiotropic | Renal tubular acidosis, distal, with progressive nerve deafness (dRTA-D) [MIM:267300] |
ATP7A | Q04656 | pleiotropic | Menkes disease (MNKD) [MIM:309400] Occipital horn syndrome (OHS) [MIM:304150] Distal spinal muscular atrophy, X-linked, 3 (DSMAX3) [MIM:300489] |
ATP7B | P35670 | non-pleiotropic | Wilson disease (WD) [MIM:277900] |
ATP8A2 | Q9NTI2 | non-pleiotropic | Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 (CMARQ4) [MIM:615268] |