|
81
|
|
|
Potassium voltage-gated channel subfamily E regulatory subunit 4 |
MIRP3 |
|
|
82
|
|
|
Kinesin family member 4A |
KIF4, KIF4G1, MRX100, TMDI, XLID100 |
|
|
83
|
|
|
3-ketodihydrosphingosine reductase |
DHSR, EKVP4, FVT1, SDR35C1 |
Alopecia, Brachydactyly, Cataract, Diabetes mellitus, Dwarfism, Erythrokeratodermia variabilis, Glaucoma, Lymphoma, Mental retardation, Microcephaly, Palmoplantar keratoderma, Palmoplantar keratosis, Patchy palmoplantar keratoderma, Platelet-type bleeding disorder, Progressive symmetric erythrokeratodermia, Skin neoplasmsView all (1 more) |
|
84
|
|
|
Kallikrein related peptidase 5 |
KLK-L2, KLKL2, SCTE |
|
|
85
|
|
|
KN motif and ankyrin repeat domains 2 |
ANKRD25, MXRA3, NPHS16, PPKWH, SIP |
|
|
86
|
|
|
Kinesin family binding protein |
KBP, KIAA1279, KIF1BP, TTC20 |
Clinodactyly, Congenital coloboma of iris, Congenital keratoglobus, Congenital microcephaly, Corneal erosion, Corneal ulcer, Cortical dysplasia, Developmental delay, Dwarfism, Goldberg-shprintzen megacolon syndrome, Hirschsprung disease, Hypoplasia of corpus callosum, Hypoplasia of the maxilla, Hypospadias, Mental retardation, Macrotia, Malformation of cortical development, Microcephaly, Microlissencephaly, Pachygyria, Polymicrogyria, Ptosis, Shprintzen-goldberg syndrome, Specific learning disorder, Syndactyly of fingers, SynophrysView all (11 more) |
|
87
|
|
|
Kelch like family member 3 |
PHA2D |
|
|
88
|
|
|
Lysine acetyltransferase 2A |
GCN5, GCN5L2, PCAF-b, hGCN5 |
|
|
89
|
|
|
Potassium voltage-gated channel subfamily H member 5 |
DEE112, EAG2, H-EAG2, Kv10.2, hEAG2 |
|
|
90
|
|
|
Kinase suppressor of ras 2 |
- |
|
