|
361
|
|
|
ATP binding cassette subfamily C member 5 |
ABC33, EST277145, MOAT-C, MOATC, MRP5, SMRP, pABC11 |
|
|
362
|
|
|
ATP binding cassette subfamily B member 6 (LAN blood group) |
ABC, LAN, MTABC3, PRP, umat |
Anemia, Breast cancer, Cafe-au-lait spot, Coloboma of eye, Coloboma of macula, Coloboma of optic disc, Microphthalmia with coloboma, Colorectal cancer, Colorectal neoplasms, Congenital coloboma of iris, Congenital ocular coloboma, Dwarfism, Dyschromatosis universalis hereditaria, Hypertension, Lens coloboma, Sclerocystic ovaries, Periodic paralysis, Polycystic ovary syndrome, Pseudohyperkalemia cardiffView all (4 more) |
|
363
|
|
|
Dynamin 1 like |
DLP1, DRP1, DVLP, DYMPLE, EMPF, EMPF1, HDYNIV, OPA5 |
Anemia, Atrophy of corpus callosum, Bilateral convulsive seizures, Brainstem atrophy, Cataract, Cerebellar atrophy, Cerebral atrophy, Color blindness, Congenital microcephaly, Dementia, Developmental delay, Diabetes mellitus, Duane retraction syndrome, Dysphagia, Encephalopathy, Epileptic encephalopathy, Hallucinations, Hearing loss, Horizontal nystagmus, Hypogonadism, Hypothyroidism, Microcephaly, Microlissencephaly, Migraine, Mitochondrial encephalomyopathy, Morning glory anomaly, Myocardial ischemia, Myoclonic seizures, Myopathy, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Optic atrophy, Parkinson disease, Ptosis, Sensorimotor neuropathy, Spastic paraplegia, Status epilepticus, Strabismus, Temporal pallor of optic discView all (25 more) |
|
364
|
|
|
Cadherin 8 |
Nbla04261 |
|
|
365
|
|
|
ATP binding cassette subfamily C member 9 |
ABC37, ATFB12, CANTU, CMD1O, IDMYS, SUR2 |
Acromegaloid facial appearance syndrome, Atrial fibrillation, Atrioventricular block, Bicuspid aortic valve, Blepharophimosis, Brugada syndrome, Bundle branch block, Cardiomyopathy, Congenital epicanthus, Congenital exomphalos, Dilated cardiomyopathy, Dysmorphic features, Endometrial neoplasms, Endometrial carcinoma, Endometrioma, Endometriosis, Gout, Gouty arthritis, Hearing loss, Hypertrichosis, Hypertrichosis-acromegaloid facial appearance syndrome, Hypertrichotic osteochondrodysplasia, Hypertrophic cardiomyopathy, Impaired myocardial contractility, Lipoatrophy, Lipodystrophy, Macrocephaly, Macroglossia, Macrostomia, Mental retardation, Micrognathism, Multiple congenital anomalies, Myopathy, Osteochondrodysplasia, Osteoporosis, Palmoplantar keratoderma, Paroxysmal atrial fibrillation, Paroxysmal ventricular tachycardia, Patent ductus arteriosus, Pericardial effusion, Sick sinus syndrome, Skeletal dysplasia, Supraventricular tachycardia, Syndactyly of fingers, Synophrys, Trifascicular block, Ventricular congenital hypertrophy, Ventricular fibrillation, Ventricular tachycardia, Wolff-parkinson-white syndromeView all (35 more) |
|
366
|
|
|
MicroRNA 4519 |
- |
|
|
367
|
|
|
MicroRNA 4516 |
mir-4516 |
|
|
368
|
|
|
MicroRNA 4482 |
MIR4482-1, hsa-mir-4482-1 |
|
|
369
|
|
|
MicroRNA 4467 |
- |
|
|
370
|
|
|
MicroRNA 2682 |
mir-2682 |
|
