|
51
|
|
|
Klotho beta |
BKL |
|
|
52
|
|
|
KH domain containing 3 like, subcortical maternal complex member |
C6orf221, ECAT1, HYDM2 |
|
|
53
|
|
|
Potassium channel tetramerization domain containing 7 |
CLN14, EPM3 |
Cerebellar ataxia, Cerebellar atrophy, Cerebral atrophy, Dementia, Developmental regression, Disorder of eye, Dysarthria, Dysphagia, Febrile seizures, Focal myoclonic seizures, High palate, Mental retardation, Microcephaly, Movement disorders, Myoclonic epilepsy, Myoclonic seizures, Neuronal ceroid lipofuscinosis, Optic atrophy, Photomyoclonic seizures, Progressive myoclonic epilepsy, Seizure, SynophrysView all (7 more) |
|
54
|
|
|
Potassium calcium-activated channel subfamily U member 1 |
KCNMC1, KCa5, KCa5.1, Kcnma3, SPGF79, Slo3 |
|
|
55
|
|
|
KIAA1958 |
- |
|
|
56
|
|
|
KN motif and ankyrin repeat domains 4 |
ANKRD38, dJ1078M7.1 |
|
|
57
|
|
|
Potassium voltage-gated channel modifier subfamily V member 2 |
KV11.1, Kv8.2, RCD3B |
Astigmatism, Cone dystrophy, Cone dystrophy with supernormal rod response, Cone-rod dystrophy, Disorder of eye, Horizontal nystagmus, Myopia, Nyctalopia, Progressive cone dystrophy, Retinal cone dystrophy, Retinal dystrophy, Stargardt disease |
|
58
|
|
|
Keratinocyte associated protein 3 |
KCP3 |
|
|
59
|
|
|
Kelch domain containing 8B |
CHL |
|
|
60
|
|
|
KH RNA binding domain containing, signal transduction associated 2 |
KHDRBS2-OT, KHDRBS2-OT1, SLM-1, SLM1 |
|
