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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Statistics

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

pleiotropic

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]