|
261
|
|
|
Potassium channel tetramerization domain containing 15 |
- |
|
|
262
|
|
|
KLF3 antisense RNA 1 |
- |
|
|
263
|
|
|
Potassium channel tetramerization domain containing 17 |
- |
Anxiety disorder, Blepharospasm, Dysarthria, Laryngeal dystonia, Mental depression, Myoclonic dystonia, Myoclonus-dystonia syndrome, Obsessive-compulsive disorder, Panic disorder, Personality disorders, Spinal cord myoclonus, Writer`s cramp |
|
264
|
|
|
Lysine demethylase 8 |
JMJD5 |
|
|
265
|
|
|
KIAA0319 like |
AAVR, AAVRL |
|
|
266
|
|
|
Lysine acetyltransferase 6A |
ARTHS, MOZ, MRD32, MYST-3, MYST3, RUNXBP2, ZC2HC6A, ZNF220 |
Accessory nipple, Adenocarcinoma, Atrial septal defect, Brachydactyly, Congenital alveolar dysplasia, Camptodactyly of fingers, Central visual impairment, Congenital epicanthus, Congenital malrotation of intestine, Craniosynostosis, Cryptorchidism, Developmental delay, Dwarfism, Gastroesophageal reflux disease, Hemangioma, Hydronephrosis, Mental retardation, Intellectual disability-craniofacial anomalies-cardiac defects syndrome, Laryngomalacia, Medulloblastoma, Medullomyoblastoma, Microcephaly, Myeloid leukemia with t(8;16)(p11;p13) translocation, Hypotonia, Optic atrophy, Patent ductus arteriosus, Plagiocephaly, Posteriorly rotated ear, Prostatic neoplasms, Prostate cancer, Ptosis, Strabismus, Ventricular septal defectView all (18 more) |
|
267
|
|
|
Kelch like family member 15 |
HEL-S-305, XLID103 |
|
|
268
|
|
|
Potassium voltage-gated channel interacting protein 4 |
CALP, KCHIP4 |
|
|
269
|
|
|
Lysine methyltransferase 2D |
AAD10, ALR, BCAHH, CAGL114, KABUK1, KMS, MLL2, MLL4, TNRC21 |
Abnormal dermatoglyphic pattern, Anemia, Aortic coarctation, Atrial septal defect, Bipolar disorder, Bladder neoplasm, Breast cancer, Breast carcinoma, Cavernous sinus meningioma, Cerebral cortical atrophy, Complement component deficiency, Congenital diaphragmatic hernia, Congenital hypoplasia of penis, Congenital hypothyroidism, Congenital malrotation of intestine, Congenital ocular coloboma, Cryptorchidism, Cystosarcoma phyllodes, Developmental delay, Developmental dysplasia of the hip, Diffuse lymphoma, Dwarfism, Dysmorphic features, Ectopic kidney, Esophagus neoplasm, Hearing loss, Heart septal defects, Hereditary paraganglioma-pheochromocytoma syndromes, High palate, Hydrocephalus, Hydronephrosis, Hypodontia, Hypospadias, Hypotonia, Immune thrombocytopenic purpura, Imperforate anus, Kabuki syndrome, Lupus erythematosus, Lymphoma, Macrotia, Malabsorption syndrome, Mammary neoplasms, Marfan syndrome, Mental retardation, Microcephaly, Microcornea, Microdontia, Microphthalmos, Microtia, Movement disorders, Multiple congenital anomalies, Multiple myeloma, Nystagmus, Obesity, Otitis media, Penis agenesis, Phyllodes tumor, Posteriorly rotated ear, Precocious puberty, Prostate cancer, Prostatic neoplasms, Ptosis, Scoliosis, Sezary syndrome, Strabismus, Submucous cleft of soft and hard palate, T-cell lymphoma, Urinary bladder cancer, Ventricular septal defectView all (54 more) |
|
270
|
|
|
Lysine demethylase 7A |
JHDM1D |
|
