|
401
|
|
|
Ankyrin 2 |
ANK-2, CFAP87, FAP87, LQT4, brank-2 |
Atrial fibrillation, Breast cancer, Brugada syndrome, Cardiac arrhythmia, Catecholaminergic polymorphic ventricular tachycardia, Colorectal cancer, Dysautonomia, Leukemia, Long qt syndrome, Neurodevelopmental disorders, Romano-ward syndrome, Stroke, Torsades de pointes |
|
402
|
|
|
Ankyrin 3 |
ANKYRIN-G, MRT37 |
Amyotrophic lateral sclerosis, Anhedonia, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Depressed bipolar disorder, Development disorder, Grand mal status epilepticus, Intellectual disability-sleep disturbance syndrome, Lateral sclerosis, Leukemia, Lung neoplasms, Lung cancer, Macrocephaly, Manic disorder, Mental depression, Mental retardation, Mood disorder, Nonconvulsive status epilepticus, Nonorganic psychosis, Petit mal status, Progeria, Psychosis, Schizophrenia, Status epilepticus, Transient psychotic disorderView all (11 more) |
|
403
|
|
|
Adipogenesis associated Mth938 domain containing |
C11orf67, CK067, PTD015 |
|
|
404
|
|
|
Acyl-CoA dehydrogenase family member 9 |
MC1DN20, NPD002 |
Acyl coa dehydrogenase deficiency, Cardiomyopathy, Congestive heart failure, Epileptic encephalopathy, Fatty liver, Hypertrophic cardiomyopathy, Hypoglycemia, Liver failure, Mitochondrial complex deficiency, Myasthenia gravis, Stroke |
|
405
|
|
|
ABR activator of RhoGEF and GTPase |
MDB |
|
|
406
|
|
|
Alanyl aminopeptidase, membrane |
AP-M, AP-N, APN, CD13, GP150, LAP1, P150, PEPN, hAPN |
|
|
407
|
|
|
Rho GTPase activating protein 35 |
GRF-1, GRLF1, P190-A, P190A, p190ARhoGAP, p190RhoGAP |
|
|
408
|
|
|
Ankyrin repeat domain containing 11 |
ANCO-1, ANCO1, LZ16, T13 |
16q24.3 microdeletion syndrome, Astigmatism, Atrioventricular septal defect, Autism spectrum disorder, Autism, Brachydactyly, Camptodactyly of fingers, Carcinoma, Cardiomyopathy, Clinodactyly, Colpocephaly, Congenital epicanthus, Rib fusion, Congenital malformation of the left heart, Cryptorchidism, Dermatitis, Developmental delay, Developmental regression, Dwarfism, Dysmorphic features, Dysphagia, Epilepsy, Esophageal varix, Esotropia, Excessive tearing, Frontal bossing, Fused incisors, Hearing loss, High palate, Hyperopia, Hypodontia, Hypoplasia of corpus callosum, Hypoplasia of the optic nerve, Kbg syndrome, Macrodontia, Macrostomia, Macrotia, Malocclusion, Melanoma, Mental retardation, Metabolic bone disorder, Microcephaly, Micrognathism, Multiple congenital anomalies, Myopia, Neck webbing, Neurodevelopmental disorders, Nystagmus, Oligodontia, Osteopenia, Otitis media, Periventricular nodular heterotopia, Portal hypertension, Ptosis, Salaam seizures, Scoliosis, Strabismus, Syndactyly, Synophrys, Ventricular septal defectView all (45 more) |
|
409
|
|
|
Activator of basal transcription 1 |
Esf2, hABT1 |
|
|
410
|
|
|
ALG6 alpha-1,3-glucosyltransferase |
CDG1C |
|
