Found 257 pleiotropic proteins (16.0 %) and 1345 non-pleiotropic proteins (84.0 %).
1602 items found (page 29 of 33)
| Gene | UniProt | Protein Type | Disease |
|---|---|---|---|
| STAMBP | O95630 | non-pleiotropic | Microcephaly-capillary malformation syndrome (MICCAP) [MIM:614261] |
| STAR | P49675 | non-pleiotropic | Adrenal hyperplasia 1 (AH1) [MIM:201710] |
| STAT1 | P42224 | pleiotropic | STAT1 deficiency complete (STAT1D) [MIM:613796] Mendelian susceptibility to mycobacterial disease (MSMD) [MIM:209950] Candidiasis, familial, 7 (CANDF7) [MIM:614162] |
| STAT3 | P40763 | non-pleiotropic | Hyperimmunoglobulin E recurrent infection syndrome, autosomal dominant (AD-HIES) [MIM:147060] |
| STAT5B | P51692 | non-pleiotropic | Growth hormone insensitivity with immunodeficiency (GHII) [MIM:245590] |
| STIM1 | Q13586 | pleiotropic | Myopathy, tubular aggregate (TAM) [MIM:160565] Immunodeficiency 10 (IMD10) [MIM:612783] |
| STK10 | O94804 | non-pleiotropic | Testicular germ cell tumor (TGCT) [MIM:273300] |
| STK11 | Q15831 | pleiotropic | Peutz-Jeghers syndrome (PJS) [MIM:175200] Testicular germ cell tumor (TGCT) [MIM:273300] |
| STOX1 | Q6ZVD7 | non-pleiotropic | Pre-eclampsia/eclampsia 4 (PEE4) [MIM:609404] |
| STS | P08842 | non-pleiotropic | Ichthyosis, X-linked (IXL) [MIM:308100] |
| STT3A | P46977 | non-pleiotropic | Congenital disorder of glycosylation 1W (CDG1W) [MIM:615596] |
| STXBP1 | P61764 | non-pleiotropic | Epileptic encephalopathy, early infantile, 4 (EIEE4) [MIM:612164] |
| STXBP2 | Q15833 | non-pleiotropic | Familial hemophagocytic lymphohistiocytosis 5 (FHL5) [MIM:613101] |
| SUCLA2 | Q9P2R7 | non-pleiotropic | Mitochondrial DNA depletion syndrome 5 (MTDPS5) [MIM:612073] |
| SUCLG1 | P53597 | non-pleiotropic | Mitochondrial DNA depletion syndrome 9 (MTDPS9) [MIM:245400] |
| SUGCT | Q9HAC7 | non-pleiotropic | Glutaric aciduria 3 (GA3) [MIM:231690] |
| SUMF1 | Q8NBK3 | non-pleiotropic | Multiple sulfatase deficiency (MSD) [MIM:272200] |
| SUOX | P51687 | non-pleiotropic | Isolated sulfite oxidase deficiency (ISOD) [MIM:272300] |
| SURF1 | Q15526 | non-pleiotropic | Leigh syndrome (LS) [MIM:256000] |
| SYNE2 | Q8WXH0 | non-pleiotropic | Emery-Dreifuss muscular dystrophy 5, autosomal dominant (EDMD5) [MIM:612999] |
| SYNGAP1 | Q96PV0 | non-pleiotropic | Mental retardation, autosomal dominant 5 (MRD5) [MIM:612621] |
| SYNJ1 | O43426 | non-pleiotropic | Parkinson disease 20, early-onset (PARK20) [MIM:615530] |
| SYP | P08247 | non-pleiotropic | Mental retardation, X-linked, SYP-related (MRXSYP) [MIM:300802] |
| SYT14 | Q8NB59 | non-pleiotropic | Spinocerebellar ataxia, autosomal recessive, 11 (SCAR11) [MIM:614229] |
| TAB2 | Q9NYJ8 | non-pleiotropic | Congenital heart defects, multiple types, 2 (CHTD2) [MIM:614980] |
| TAC3 | Q9UHF0 | non-pleiotropic | Hypogonadotropic hypogonadism 10 with or without anosmia (HH10) [MIM:614839] |
| TACR3 | P29371 | non-pleiotropic | Hypogonadotropic hypogonadism 11 with or without anosmia (HH11) [MIM:614840] |
| TAF2 | Q6P1X5 | non-pleiotropic | Mental retardation, autosomal recessive 40 (MRT40) [MIM:615599] |
| TAT | P17735 | non-pleiotropic | Tyrosinemia 2 (TYRSN2) [MIM:276600] |
| TAZ | Q16635 | non-pleiotropic | Barth syndrome (BTHS) [MIM:302060] |
| TBC1D24 | Q9ULP9 | pleiotropic | Familial infantile myoclonic epilepsy (FIME) [MIM:605021] Epileptic encephalopathy, early infantile, 16 (EIEE16) [MIM:615338] Deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures syndrome (DOORS) [MIM:220500] Deafness, autosomal recessive, 86 (DFNB86) [MIM:614617] |
| TBX1 | O43435 | pleiotropic | DiGeorge syndrome (DGS) [MIM:188400] Conotruncal heart malformations (CTHM) [MIM:217095] Velocardiofacial syndrome (VCFS) [MIM:192430] |
| TBX19 | O60806 | non-pleiotropic | ACTH deficiency, isolated (IAD) [MIM:201400] |
| TBX20 | Q9UMR3 | non-pleiotropic | Atrial septal defect 4 (ASD4) [MIM:611363] |
| TBX3 | O15119 | non-pleiotropic | Ulnar-mammary syndrome (UMS) [MIM:181450] |
| TBX4 | P57082 | non-pleiotropic | Small patella syndrome (SPS) [MIM:147891] |
| TBX5 | Q99593 | non-pleiotropic | Holt-Oram syndrome (HOS) [MIM:142900] |
| TBXA2R | P21731 | non-pleiotropic | Bleeding disorder, platelet-type 13 (BDPLT13) [MIM:614009] |
| TCF12 | Q99081 | non-pleiotropic | Craniosynostosis 3 (CRS3) [MIM:615314] |
| TCF4 | P15884 | non-pleiotropic | Pitt-Hopkins syndrome (PTHS) [MIM:610954] |
| TCIRG1 | Q13488 | non-pleiotropic | Osteopetrosis, autosomal recessive 1 (OPTB1) [MIM:259700] |
| TCOF1 | Q13428 | non-pleiotropic | Treacher Collins syndrome 1 (TCS1) [MIM:154500] |
| TDP1 | Q9NUW8 | non-pleiotropic | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy (SCAN1) [MIM:607250] |
| TEAD1 | P28347 | non-pleiotropic | Sveinsson chorioretinal atrophy (SCRA) [MIM:108985] |
| TECR | Q9NZ01 | non-pleiotropic | Mental retardation, autosomal recessive 14 (MRT14) [MIM:614020] |
| TEK | Q02763 | non-pleiotropic | Dominantly inherited venous malformations (VMCM) [MIM:600195] |
| TERT | O14746 | pleiotropic | Dyskeratosis congenita, autosomal recessive, 4 (DKCB4) [MIM:613989] Pulmonary fibrosis, and/or bone marrow failure, telomere-related, 1 (PFBMFT1) [MIM:614742] Dyskeratosis congenita, autosomal dominant, 2 (DKCA2) [MIM:613989] |
| TF | P02787 | non-pleiotropic | Atransferrinemia (ATRAF) [MIM:209300] |
| TFAP2A | P05549 | non-pleiotropic | Branchiooculofacial syndrome (BOFS) [MIM:113620] |
| TFAP2B | Q92481 | non-pleiotropic | Char syndrome (CHAR) [MIM:169100] |