|
241
|
|
|
Kallikrein related peptidase 10 |
NES1, PRSSL1 |
|
|
242
|
|
|
Kinesin family member 15 |
BRDCS2, HKLP2, KLP2, KNSL7, NY-BR-62 |
21q22.11q22.12 microdeletion syndrome, Agenesis of corpus callosum, Anemia, Atrial septal defect, Bipolar disorder, Brachydactyly, Clinodactyly, Congenital camptodactyly, Dwarfism, Glomerulonephritis, Hypoplasia of nipple, Liver carcinoma, Mental retardation, Microcephaly, Microtia, Nail dystrophy, Otitis media, Scaphocephaly, Stereotypy, StrabismusView all (5 more) |
|
243
|
|
|
Kinetochore scaffold 1 |
AF15Q14, CASC5, CT29, D40, MCPH4, PPP1R55, Spc7, hKNL-1, hSpc105 |
Agenesis of corpus callosum, Developmental delay, Dwarfism, Mental retardation, Microcephaly, Micrognathism, Mirror movements, Neuronal heterotopia, Pachygyria, Prostate cancer, Prostate cancer, hereditary, Renal aplasia, Synophrys, Vesicoureteral reflux |
|
244
|
|
|
Lysine acetyltransferase 14 |
ATAC2, CRP2BP, CSRP2BP, PRO1194, dJ717M23.1 |
|
|
245
|
|
|
Kinase D interacting substrate 220 |
ARMS, SINO, VENARG |
Astigmatism, Cerebral atrophy, Congenital epicanthus, Developmental delay, Esophoria, Esotropia, Hyperopia, Hypoplasia of corpus callosum, Mental retardation, Nystagmus, Obesity, Plagiocephaly, Spastic paraplegia, Spastic paraplegia, intellectual disability, nystagmus, and obesity |
|
246
|
|
|
Kinesin family member 17 |
KIF17B, KIF3X, KLP-2, OSM-3 |
|
|
247
|
|
|
Potassium sodium-activated channel subfamily T member 1 |
DEE14, EIEE14, ENFL5, KCa4.1, KNa1.1, SLACK, Slo2.2, bA100C15.2 |
Amygdalo-hippocampal epilepsy, Benign occipital epilepsy, Cerebral cortical atrophy, Development disorder, Developmental regression, Digestive epilepsy, Epilepsy, Epileptic encephalopathy, Focal epilepsy, Histiocytic medullary reticulosis, Hypoplasia of corpus callosum, Impaired cognition, Malignant migrating partial seizures of infancy, Mental depression, Microcephaly, Migrating partial seizures in infancy, Nocturnal epilepsy, Panayiotopoulos syndrome, Rhinencephalic epilepsy, Quadriplegia, Seizure, Status epilepticus, Subclinical seizureView all (8 more) |
|
248
|
|
|
KIAA1549 |
RP86 |
Anaplastic astrocytoma, Astrocytoma, Cataract, Congenital hypoplasia of penis, Diabetes mellitus, Fibrillary astrocytoma, Gemistocytic astrocytoma, Glaucoma, Grade i astrocytoma, Hearing loss, Hyperinsulinism, Hypogonadism, Intracranial astrocytoma, Keratoconus, Mental retardation, Nystagmus, Obesity, Oligoastrocytoma, Optic atrophy, Pilomyxoid astrocytoma, Protoplasmic astrocytoma, Retinitis pigmentosaView all (7 more) |
|
249
|
|
|
Lysine methyltransferase 2C |
HALR, KLEFS2, MLL3 |
Adenocarcinoma, Arnold-chiari malformation, Autism, Urinary bladder cancer, Bladder neoplasm, Carcinoma, Cholangiocarcinoma, Colorectal cancer, Developmental delay, Esophagus neoplasm, Gastric cancer, Intrahepatic cholangiocarcinoma, Kleefstra syndrome, Leukemia, Liver carcinoma, Mental retardation, Microcephaly, Myeloid leukemia, Neurodevelopmental disorders, Obsolete prominent epicanthal folds, Prostatic neoplasms, Prostate cancer, Sezary syndrome, Stomach neoplasmsView all (9 more) |
|
250
|
|
|
Lysine demethylase 5A |
NEDEHC, RBBP-2, RBBP2, RBP2 |
|
