|
271
|
|
|
Potassium voltage-gated channel subfamily H member 6 |
ERG-2, ERG2, HERG2, Kv11.2, hERG-2 |
|
|
272
|
|
|
Kinesin family member 18A |
MS-KIF18A, PPP1R99 |
|
|
273
|
|
|
Lysine demethylase 5C |
DXS1272E, JARID1C, MRX13, MRXJ, MRXS16, MRXSCJ, MRXSJ, SMCX, XE169 |
Alopecia areata, Autism, Brachydactyly, Cafe-au-lait spot, Chromophobe carcinoma, Clinodactyly, Congenital clubfoot, Congenital pectus excavatum, Congenital torticollis, Cryptorchidism, Developmental delay, Distal lower limb amyotrophy, Dwarfism, Dysmorphic features, Epilepsy, High palate, Hyperopia, Hypoplasia of the maxilla, Hypothyroidism, Mental retardation, Macrocephaly, Macrotia, Malocclusion, Microcephaly, Micrognathism, Movement disorders, Myopia, Papillary renal carcinoma, Partington syndrome, Penis agenesis, Plagiocephaly, Renal carcinoma, Spastic paraplegia, Strabismus, Syndromic mental retardation, x-linked, Talipes calcaneovalgusView all (21 more) |
|
274
|
|
|
Lysine demethylase 5D |
HY, HYA, JARID1D, SMCY |
|
|
275
|
|
|
Killer cell lectin like receptor C4 |
NKG2-F, NKG2F |
Acne, Anorexia, Aortic valve insufficiency, Aphthous ulcer, Arthritis, Behcet syndrome, Cataract, Cranial nerve paralysis, Developmental regression, Encephalitis, Endocarditis, Gangrene, Keratoconjunctivitis sicca, Lymphocytic leukemia, Malabsorption syndrome, Migraine, Myocardial infarction, Myositis, Oral ulcer, Pancreatitis, Pericarditis, Pleural effusion, Pleuritis, Renal glomerular disease, Renal insufficiency, Retinal diseases, Retrobulbar neuritis, VasculitisView all (13 more) |
|
276
|
|
|
Katanin catalytic subunit A1 like 2 |
- |
|
|
277
|
|
|
Potassium two pore domain channel subfamily K member 16 |
K2p16.1, TALK-1, TALK1 |
|
|
278
|
|
|
Potassium channel tetramerization domain containing 10 |
BTBD28, MSTP028, ULRO61, hBACURD3 |
|
|
279
|
|
|
Kringle containing transmembrane protein 1 |
ECTD13, KREMEN, KRM1 |
|
|
280
|
|
|
Kirre like nephrin family adhesion molecule 2 |
FILTRIN, NEPH3, NLG1 |
|
