Found 257 pleiotropic proteins (16.0 %) and 1345 non-pleiotropic proteins (84.0 %).
1602 items found (page 16 of 33)
| Gene | UniProt | Protein Type | Disease |
|---|---|---|---|
| KCNQ3 | O43525 | non-pleiotropic | Seizures, benign familial neonatal 2 (BFNS2) [MIM:121201] |
| KCNQ4 | P56696 | non-pleiotropic | Deafness, autosomal dominant, 2A (DFNA2A) [MIM:600101] |
| KCNV2 | Q8TDN2 | non-pleiotropic | Cone dystrophy retinal 3B (RCD3B) [MIM:610356] |
| KCTD1 | Q719H9 | non-pleiotropic | Scalp-ear-nipple syndrome (SENS) [MIM:181270] |
| KCTD7 | Q96MP8 | non-pleiotropic | Epilepsy, progressive myoclonic 3, with or without intracellular inclusions (EPM3) [MIM:611726] |
| KDM5C | P41229 | non-pleiotropic | Mental retardation, X-linked, syndromic, Claes-Jensen type (MRXSCJ) [MIM:300534] |
| KERA | O60938 | non-pleiotropic | The autosomal recessive cornea plana 2 (CNA2) [MIM:217300] |
| KHK | P50053 | non-pleiotropic | Fructosuria (FRUCT) [MIM:229800] |
| KIAA0196 | Q12768 | non-pleiotropic | Spastic paraplegia 8, autosomal dominant (SPG8) [MIM:603563] |
| KIF11 | P52732 | non-pleiotropic | Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR) [MIM:152950] |
| KIF1A | Q12756 | pleiotropic | Mental retardation, autosomal dominant 9 (MRD9) [MIM:614255] Spastic paraplegia 30, autosomal recessive (SPG30) [MIM:610357] |
| KIF1C | O43896 | non-pleiotropic | Spastic ataxia 2, autosomal recessive (SPAX2) [MIM:611302] |
| KIF22 | Q14807 | non-pleiotropic | Spondyloepimetaphyseal dysplasia with joint laxity, 2 (SEMDJL2) [MIM:603546] |
| KIF2A | O00139 | non-pleiotropic | Cortical dysplasia, complex, with other brain malformations 3 (CDCBM3) [MIM:615411] |
| KIF5A | Q12840 | non-pleiotropic | Spastic paraplegia 10, autosomal dominant (SPG10) [MIM:604187] |
| KIF5C | O60282 | non-pleiotropic | Cortical dysplasia, complex, with other brain malformations 2 (CDCBM2) [MIM:615282] |
| KIF7 | Q2M1P5 | pleiotropic | Pallister-Hall syndrome (PHS) [MIM:146510] Bardet-Biedl syndrome (BBS) [MIM:209900] Acrocallosal syndrome (ACLS) [MIM:200990] Hydrolethalus syndrome 2 (HLS2) [MIM:614120] |
| KIRREL3 | Q8IZU9 | non-pleiotropic | Mental retardation, autosomal dominant 4 (MRD4) [MIM:612581] |
| KISS1 | Q15726 | non-pleiotropic | Hypogonadotropic hypogonadism 13 with or without anosmia (HH13) [MIM:614842] |
| KISS1R | Q969F8 | pleiotropic | Hypogonadotropic hypogonadism 8 with or without anosmia (HH8) [MIM:614837] Precocious puberty, central 1 (CPPB1) [MIM:176400] |
| KIT | P10721 | pleiotropic | Piebald trait (PBT) [MIM:172800] Gastrointestinal stromal tumor (GIST) [MIM:606764] |
| KL | Q9UEF7 | non-pleiotropic | Tumoral calcinosis, hyperphosphatemic, familial (HFTC) [MIM:211900] |
| KLF11 | O14901 | non-pleiotropic | Maturity-onset diabetes of the young 7 (MODY7) [MIM:610508] |
| KLHL10 | Q6JEL2 | non-pleiotropic | Spermatogenic failure 11 (SPGF11) [MIM:615081] |
| KLHL3 | Q9UH77 | non-pleiotropic | Pseudohypoaldosteronism 2D (PHA2D) [MIM:614495] |
| KLHL40 | Q2TBA0 | non-pleiotropic | Nemaline myopathy 8 (NEM8) [MIM:615348] |
| KLHL7 | Q8IXQ5 | non-pleiotropic | Retinitis pigmentosa 42 (RP42) [MIM:612943] |
| KLKB1 | P03952 | non-pleiotropic | Prekallikrein deficiency (PKK deficiency) [MIM:612423] |
| KRAS | P01116 | pleiotropic | Gastric cancer (GASC) [MIM:613659] Noonan syndrome 3 (NS3) [MIM:609942] Cardiofaciocutaneous syndrome 2 (CFC2) [MIM:615278] |
| KRIT1 | O00522 | non-pleiotropic | Cerebral cavernous malformations 1 (CCM1) [MIM:116860] |
| KRT12 | Q99456 | non-pleiotropic | Corneal dystrophy, Meesmann (MECD) [MIM:122100] |
| KRT13 | P13646 | non-pleiotropic | White sponge nevus 2 (WSN2) [MIM:615785] |
| KRT17 | Q04695 | pleiotropic | Pachyonychia congenita 2 (PC2) [MIM:167210] Steatocystoma multiplex (SM) [MIM:184500] |
| KRT18 | P05783 | non-pleiotropic | Cirrhosis (CIRRH) [MIM:215600] |
| KRT2 | P35908 | non-pleiotropic | Ichthyosis bullosa of Siemens (IBS) [MIM:146800] |
| KRT3 | P12035 | non-pleiotropic | Corneal dystrophy, Meesmann (MECD) [MIM:122100] |
| KRT4 | P19013 | non-pleiotropic | White sponge nevus 1 (WSN1) [MIM:193900] |
| KRT6A | P02538 | non-pleiotropic | Pachyonychia congenita 1 (PC1) [MIM:167200] |
| KRT6B | P04259 | non-pleiotropic | Pachyonychia congenita 2 (PC2) [MIM:167210] |
| KRT74 | Q7RTS7 | pleiotropic | Woolly hair autosomal dominant (ADWH) [MIM:194300] Hypotrichosis 3 (HYPT3) [MIM:613981] |
| KRT75 | O95678 | non-pleiotropic | Loose anagen hair syndrome (LAHS) [MIM:600628] |
| KRT8 | P05787 | non-pleiotropic | Cirrhosis (CIRRH) [MIM:215600] |
| KRT81 | Q14533 | non-pleiotropic | Monilethrix (MLTRX) [MIM:158000] |
| KRT83 | P78385 | non-pleiotropic | Monilethrix (MLTRX) [MIM:158000] |
| KRT85 | P78386 | non-pleiotropic | Ectodermal dysplasia 4, hair/nail type (ECTD4) [MIM:602032] |
| KRT86 | O43790 | non-pleiotropic | Monilethrix (MLTRX) [MIM:158000] |
| KRT9 | P35527 | non-pleiotropic | Keratoderma, palmoplantar, epidermolytic (EPPK) [MIM:144200] |
| L2HGDH | Q9H9P8 | non-pleiotropic | L-2-hydroxyglutaric aciduria (L2HGA) [MIM:236792] |
| LAMA4 | Q16363 | non-pleiotropic | Cardiomyopathy, dilated 1JJ (CMD1JJ) [MIM:615235] |
| LAMC3 | Q9Y6N6 | non-pleiotropic | Cortical malformations occipital (OCCM) [MIM:614115] |