231
|
|
|
Kinesin family member 16B |
C20orf23, KISC20ORF, SNX23 |
|
232
|
|
|
KAT8 regulatory NSL complex subunit 3 |
KIAA1310, NSL3, Rcd1 |
|
233
|
|
|
Lysine demethylase 3A |
JHDM2A, JHMD2A, JMJD1, JMJD1A, TSGA |
|
234
|
|
|
Kizuna centrosomal protein |
C20orf19, HT013, Kizuna, NCRNA00153, PLK1S1, RP69 |
Cataract, Congenital hypoplasia of penis, Development disorder, Diabetes mellitus, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Mental retardation, Nystagmus, Obesity, Optic atrophy, Retinitis pigmentosa, Rod-cone dystrophy |
235
|
|
|
Lysine methyltransferase 2E (inactive) |
HDCMC04P, MLL5, NKp44L, ODLURO, SETD5B |
Anxiety disorder, Autism, Cerebral cortical atrophy, Cryptorchidism, Development disorder, Developmental delay, Dolichocephaly, Epilepsy, Leukemia, Leukoencephalopathy, Macrocephaly, Macrotia, Mental depression, Mental retardation, Monocytic leukemia, Myeloid leukemia, Neurodevelopmental disorders, Skin-picking, Syndromic mental retardationView all (4 more) |
236
|
|
|
Kelch like family member 9 |
- |
|
237
|
|
|
Kelch like family member 7 |
CISS3, KLHL6, PERCHING, SBBI26 |
Accessory nipple, Bohring-opitz syndrome, Cataract, Cerebral cortical atrophy, Clinodactyly, Cold-induced sweating syndrome, Congenital camptodactyly, Congenital hypoplasia of penis, Congenital malrotation of intestine, Crisponi syndrome, Dandy-walker syndrome, Developmental delay, Diabetes mellitus, Disorder of eye, Distal arthrogryposis, Dysphagia, Gastroesophageal reflux disease, Glaucoma, Hearing loss, High palate, Hyperinsulinism, Hypogonadism, Hypoplasia of corpus callosum, Mental retardation, Keratoconus, Microcephaly, Multicystic renal dysplasia, Myopia, Nystagmus, Obesity, Optic atrophy, Phakomatosis pigmentovascularis, Proptosis, Ptosis, Retinal diseases, Retinitis pigmentosa, Rod-cone dystrophy, Strabismus, Synophrys, Talipes, Testicular hydrocele, TrigonocephalyView all (27 more) |
238
|
|
|
KIAA1217 |
ETL4, SKT |
|
239
|
|
|
Kynurenine aminotransferase 3 |
CCBL2, KAT3, KATIII |
|
240
|
|
|
Potassium voltage-gated channel subfamily Q member 5 |
Kv7.5, MRD46 |
|