|
221
|
|
|
Keratin 76 |
HUMCYT2A, KRT2B, KRT2P |
|
|
222
|
|
|
KLF transcription factor 13 |
BTEB3, FKLF2, NSLP1, RFLAT-1, RFLAT1 |
|
|
223
|
|
|
Lysine demethylase 3B |
5qNCA, C5orf7, DIJOS, JMJD1B, NET22 |
|
|
224
|
|
|
Keratin 20 |
CD20, CK-20, CK20, K20, KRT21 |
|
|
225
|
|
|
Kinesin family member 1A |
ATSV, C2orf20, HSN2C, MRD9, NESCAVS, SPG30, SPG30A, SPG30B, UNC104 |
Acquired porencephaly, Acrosteolysis, Amyloid angiopathy, Anhidrosis, Arthrogryposis multiplex congenita, Atrophy of corpus callosum, Autism, Brainstem atrophy, Cerebellar atrophy, Cerebral atrophy, Cerebral cortical atrophy, Congenital epicanthus, Development disorder, Developmental delay, Diabetes mellitus, Distal amyotrophy, Dysautonomia, Gastroesophageal reflux disease, Hereditary sensory and autonomic neuropathy, Hydrocephalus, Hypoplasia of corpus callosum, Infantile spasms, Mental retardation, Macrotia, Microcephaly, Micropenis, Movement disorders, Multiple congenital anomalies, Nervous system diseases, Neuropathy, Non-syndromic intellectual disability, Optic atrophy, Optic neuropathy, Paronychia inflammation, Peho syndrome, Peripheral axonal neuropathy, Peripheral neuropathy, Porencephalic cyst, Scoliosis, Sensorimotor neuropathy, Spastic paraplegia, West syndromeView all (27 more) |
|
226
|
|
|
Kelch like family member 24 |
CMH29, DRE1, EBS6, EBSSH, KRIP6 |
|
|
227
|
|
|
Kinesin family member 26B |
- |
|
|
228
|
|
|
Kelch like family member 26 |
- |
|
|
229
|
|
|
Kallikrein related peptidase 15 |
ACO, HSRNASPH |
|
|
230
|
|
|
Kinesin family member 21A |
CFEOM1, FEOM1, FEOM3A |
|
