|
281
|
|
|
Lysine acetyltransferase 8 |
LIGOWS, MOF, MYST1, ZC2HC8, hMOF |
Alzheimer disease, Anxiety disorder, Autism, Cardiovascular abnormalities, Congestive heart failure, Developmental delay, Heart failure, Hypertrophic cardiomyopathy, Mental retardation, Myocardial infarction, Schizophrenia |
|
282
|
|
|
Kelch repeat and BTB domain containing 8 |
TA-KRP, TAKRP |
|
|
283
|
|
|
KLF transcription factor 11 |
FKLF, FKLF1, MODY7, TIEG2, Tieg3 |
Hyperinsulinemic hypoglycemia, Pancreatic hypoplasia, Diabetes mellitus, Exocrine pancreatic insufficiency, Hepatocellular adenoma, Hyperglycemia, Hypoinsulinemia, Kidney disease, Mason type diabetes, Monogenic diabetes, Hypoglycemia, Obesity, Renal cyst, Retinal diseases |
|
284
|
|
|
Kirre like nephrin family adhesion molecule 3 |
KIRRE, MRD4, NEPH2, PRO4502 |
|
|
285
|
|
|
KISS1 receptor |
AXOR12, CPPB1, GPR54, HH8, HOT7T175, KISS-1R |
Anxiety disorder, Azoospermia, Central precocious puberty, Congenital camptodactyly, Breast hypoplasia, Hypoplasia of the ovary, Congenital sensorineural hearing loss, Cryptorchidism, Dwarfism, Dysarthria, Erectile dysfunction, Female hypogonadism syndrome, Gastric cancer, Gonadotropin deficiency, Gynecomastia, Hearing loss, Hypogonadism, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypopituitarism, Ichthyosis, Kallmann syndrome, Mental depression, Mirror movements, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Penis agenesis, Physiologic amenorrhea, Precocious puberty, Ptosis, Renal agenesis, Secondary physiologic amenorrhea, Skeletal dysplasia, Stomach neoplasms, Testicular hypogonadism, TestotoxicosisView all (27 more) |
|
286
|
|
|
Lysine demethylase 2B |
CXXC2, FBXL10, Fbl10, JHDM1B, PCCX2 |
|
|
287
|
|
|
Potassium voltage-gated channel subfamily A regulatory beta subunit 2 |
AKR6A5, HKvbeta2, HKvbeta2.1, HKvbeta2.2, KCNA2B, KV-BETA-2 |
1p36 deletion syndrome, Agenesis of corpus callosum, Aneurysm of aortic arch, Annular pancreas, Autism, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cardiomyopathy, Cataract, Cerebral cortical atrophy, Congenital anomaly of neck, Congenital epicanthus, Rib fusion, Congenital hypoplasia of penis, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dwarfism, Dysphagia, Epilepsy, Fatty liver, Frontal bossing, Gastroesophageal reflux disease, Hearing loss, Heart septal defects, Hemiplegia/hemiparesis, Hydronephrosis, Hypogonadism, Hypospadias, Hypothyroidism, Mental retardation, Microcephaly, Microstomia, Microtia, Myopathy, Neuroblastoma, Nystagmus, Obesity, Ocular albinism, Optic atrophy, Patent ductus arteriosus, Polydactyly of toes, Renal cyst, Scoliosis, Stereotyped behavior, Strabismus, Tetralogy of fallotView all (33 more) |
|
288
|
|
|
KIAA1755 |
quo |
|
|
289
|
|
|
Kynurenine 3-monooxygenase |
dJ317G22.1 |
|
|
290
|
|
|
KH-type splicing regulatory protein |
FBP2, FUBP2, KSRP, p75 |
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