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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UniProtID Disease Name

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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]