Found 257 pleiotropic proteins (16.0 %) and 1345 non-pleiotropic proteins (84.0 %).
1602 items found (page 6 of 33)
| Gene | UniProt | Protein Type | Disease |
|---|---|---|---|
| CEACAM16 | Q2WEN9 | non-pleiotropic | Deafness, autosomal dominant, 4B (DFNA4B) [MIM:614614] |
| CELSR1 | Q9NYQ6 | non-pleiotropic | Neural tube defects (NTD) [MIM:182940] |
| CEP152 | O94986 | pleiotropic | Microcephaly 9, primary, autosomal recessive (MCPH9) [MIM:614852] Seckel syndrome 5 (SCKL5) [MIM:613823] |
| CEP164 | Q9UPV0 | non-pleiotropic | Nephronophthisis 15 (NPHP15) [MIM:614845] |
| CERKL | Q49MI3 | non-pleiotropic | Retinitis pigmentosa 26 (RP26) [MIM:608380] |
| CFD | P00746 | non-pleiotropic | Complement factor D deficiency (CFDD) [MIM:613912] |
| CFH | P08603 | pleiotropic | Complement factor H deficiency (CFHD) [MIM:609814] Hemolytic uremic syndrome atypical 1 (AHUS1) [MIM:235400] Macular degeneration, age-related, 4 (ARMD4) [MIM:610698] |
| CFI | P05156 | pleiotropic | Complement factor I deficiency (CFI deficiency) [MIM:610984] Hemolytic uremic syndrome atypical 3 (AHUS3) [MIM:612923] Macular degeneration, age-related, 13 (ARMD13) [MIM:615439] |
| CFL2 | Q9Y281 | non-pleiotropic | Nemaline myopathy 7 (NEM7) [MIM:610687] |
| CFP | P27918 | non-pleiotropic | Properdin deficiency (PFD) [MIM:312060] |
| CFTR | P13569 | pleiotropic | Cystic fibrosis (CF) [MIM:219700] Congenital bilateral absence of the vas deferens (CBAVD) [MIM:277180] |
| CHAT | P28329 | non-pleiotropic | Myasthenic syndrome, congenital, associated with episodic apnea (CMSEA) [MIM:254210] |
| CHD2 | O14647 | non-pleiotropic | Epileptic encephalopathy, childhood-onset (EEOC) [MIM:615369] |
| CHD7 | Q9P2D1 | pleiotropic | CHARGE syndrome (CHARGES) [MIM:214800] Hypogonadotropic hypogonadism 5 with or without anosmia (HH5) [MIM:612370] |
| CHEK2 | O96017 | pleiotropic | Li-Fraumeni syndrome 2 (LFS2) [MIM:609265] Prostate cancer (PC) [MIM:176807] |
| CHM | P24386 | non-pleiotropic | Choroideremia (CHM) [MIM:303100] |
| CHMP2B | Q9UQN3 | pleiotropic | Frontotemporal dementia, chromosome 3-linked (FTD3) [MIM:600795] Amyotrophic lateral sclerosis 17 (ALS17) [MIM:614696] |
| CHMP4B | Q9H444 | non-pleiotropic | Cataract 31, multiple types (CTRCT31) [MIM:605387] |
| CHN1 | P15882 | non-pleiotropic | Duane retraction syndrome 2 (DURS2) [MIM:604356] |
| CHRDL1 | Q9BU40 | non-pleiotropic | Megalocornea 1, X-linked (MGC1) [MIM:309300] |
| CHRNA1 | P02708 | pleiotropic | Myasthenic syndrome, congenital, slow-channel (SCCMS) [MIM:601462] Myasthenic syndrome, congenital, fast-channel (FCCMS) [MIM:608930] Multiple pterygium syndrome, lethal type (LMPS) [MIM:253290] |
| CHRNA2 | Q15822 | non-pleiotropic | Epilepsy, nocturnal frontal lobe, 4 (ENFL4) [MIM:610353] |
| CHRNB2 | P17787 | non-pleiotropic | Epilepsy, nocturnal frontal lobe, 3 (ENFL3) [MIM:605375] |
| CHRND | Q07001 | pleiotropic | Myasthenic syndrome, congenital, slow-channel (SCCMS) [MIM:601462] Myasthenic syndrome, congenital, fast-channel (FCCMS) [MIM:608930] Multiple pterygium syndrome, lethal type (LMPS) [MIM:253290] |
| CHST14 | Q8NCH0 | non-pleiotropic | Ehlers-Danlos syndrome, musculocontractural type 1 (EDSMC1) [MIM:601776] |
| CHST3 | Q7LGC8 | non-pleiotropic | Spondyloepiphyseal dysplasia with congenital joint dislocations (SEDC-JD) [MIM:143095] |
| CHST6 | Q9GZX3 | non-pleiotropic | Macular dystrophy, corneal, 1 (MCDC1) [MIM:217800] |
| CHSY1 | Q86X52 | non-pleiotropic | Temtamy preaxial brachydactyly syndrome (TPBS) [MIM:605282] |
| CIB2 | O75838 | pleiotropic | Usher syndrome 1J (USH1J) [MIM:614869] Deafness, autosomal recessive, 48 (DFNB48) [MIM:609439] |
| CIITA | P33076 | non-pleiotropic | Bare lymphocyte syndrome 2 (BLS2) [MIM:209920] |
| CIRH1A | Q969X6 | non-pleiotropic | North American Indian childhood cirrhosis (NAIC) [MIM:604901] |
| CLCF1 | Q9UBD9 | non-pleiotropic | Cold-induced sweating syndrome 2 (CISS2) [MIM:610313] |
| CLCNKA | P51800 | non-pleiotropic | Bartter syndrome 4B (BS4B) [MIM:613090] |
| CLDN14 | O95500 | non-pleiotropic | Deafness, autosomal recessive, 29 (DFNB29) [MIM:614035] |
| CLDN16 | Q9Y5I7 | non-pleiotropic | Hypomagnesemia 3 (HOMG3) [MIM:248250] |
| CLDN19 | Q8N6F1 | non-pleiotropic | Hypomagnesemia 5 (HOMG5) [MIM:248190] |
| CLIC2 | O15247 | non-pleiotropic | Mental retardation, X-linked, syndromic, 32 (MRXS32) [MIM:300886] |
| CLMP | Q9H6B4 | non-pleiotropic | Congenital short bowel syndrome (CSBS) [MIM:615237] |
| CLN3 | Q13286 | non-pleiotropic | Ceroid lipofuscinosis, neuronal, 3 (CLN3) [MIM:204200] |
| CLN5 | O75503 | non-pleiotropic | Ceroid lipofuscinosis, neuronal, 5 (CLN5) [MIM:256731] |
| CLPP | Q16740 | non-pleiotropic | Perrault syndrome 3 (PRLTS3) [MIM:614129] |
| CNGA1 | P29973 | non-pleiotropic | Retinitis pigmentosa 49 (RP49) [MIM:613756] |
| CNGA3 | Q16281 | non-pleiotropic | Achromatopsia 2 (ACHM2) [MIM:216900] |
| CNGB1 | Q14028 | non-pleiotropic | Retinitis pigmentosa 45 (RP45) [MIM:613767] |
| CNNM2 | Q9H8M5 | non-pleiotropic | Hypomagnesemia 6 (HOMG6) [MIM:613882] |
| CNNM4 | Q6P4Q7 | non-pleiotropic | Jalili syndrome (JALIS) [MIM:217080] |
| COA5 | Q86WW8 | non-pleiotropic | Mitochondrial complex IV deficiency (MT-C4D) [MIM:220110] |
| COASY | Q13057 | non-pleiotropic | Neurodegeneration with brain iron accumulation 6 (NBIA6) [MIM:615643] |
| COCH | O43405 | non-pleiotropic | Deafness, autosomal dominant, 9 (DFNA9) [MIM:601369] |
| COG4 | Q9H9E3 | non-pleiotropic | Congenital disorder of glycosylation 2J (CDG2J) [MIM:613489] |