411
|
|
|
Delta/notch like EGF repeat containing |
UNQ26, bet |
|
412
|
|
|
Dynein heavy chain domain 1 |
C11orf47, CCDC35, DHCD1, DNHD1L, SPGF65 |
|
413
|
|
|
DNL-type zinc finger |
C9orf151, HEP, HEP1, TIMM15, ZIM17, bA413M3.2 |
|
414
|
|
|
Dynamin 1 |
DEE31, DEE31A, DEE31B, DNM, EIEE31 |
Asthma, Attention deficit hyperactivity disorder, Cerebellar ataxia, Developmental and epileptic encephalopathy, Developmental disability, Dog diseases, Epilepsy, Global developmental delay, Insomnia, Lennox-gastaut syndrome, Neurodevelopmental disorder, Retinopathy of prematurity, Schizophrenia, West syndrome |
415
|
|
|
Dynamin 1 like |
DLP1, DRP1, DVLP, DYMPLE, EMPF, EMPF1, HDYNIV, OPA5 |
Optic atrophy, Encephalopathy due to mitochondrial and peroxisomal fission defect, Leigh syndrome, Microcephaly, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial myopathy with sideroblastic anemia, Myocardial ischemia, Myocarditis, Obesity, Parkinson disease, Spastic paraplegia |
416
|
|
|
Dynamin 2 |
CMT2M, CMTDI1, CMTDIB, DI-CMTB, DYN2, DYNII, LCCS5 |
Centronuclear myopathy, Charcot-marie-tooth disease, Obstructive pulmonary disease, Congenital deformity of clavicle, Congenital deformity of elbow, Congenital deformity of forearm, Congenital deformity of scapula, Congenital deformity of wrist, Congenital dislocation of elbow, Congenital glenohumeral joint dislocation, Congenital structural myopathy, Hyperlipidemia, Irritable bowel syndrome, Lethal congenital contracture syndrome, Moyamoya angiopathy, Myocardial infarction, Myofibrillar myopathy, Myopathy, Peripheral neuropathy, Psoriasis, Hereditary spastic paraplegia, Stroke, Venous thromboembolism, X-linked centronuclear myopathyView all (9 more) |
417
|
|
|
Dynamin 3 |
Dyna III |
Astrocytoma, Breast cancer, Dermatophytosis, Endometriosis, Kidney neoplasms, Metabolic syndrome, Moyamoya disease, Neurotic disorder, Nonalcoholic fatty liver disease, Open angle glaucoma, Ovarian cancer, Diabetes mellitus type 2, Uterine fibroid |
418
|
|
|
Dynamin binding protein |
ARHGEF36, CTRCT48, TUBA |
|
419
|
|
|
DNA methyltransferase 1 |
ADCADN, AIM, CXXC9, DNMT, HSN1E, MCMT, m.HsaI |
Anxiety disorder, Experimental arthritis, Asthma, Autism, Cerebellar ataxia with deafness and narcolepsy, Beckwith-wiedemann syndrome, Bipolar disorder, Breast neoplasms, Carcinoma, Pancreatic ductal carcinoma, Cardiovascular disease, Cerebellar ataxia, Cerebellar ataxia, deafness, and narcolepsy, Cerebellar atrophy, Cerebral atrophy, Charcot-marie-tooth disease, Chorea, Renal cell carcinoma, Colonic neoplasms, Deglutition disorder, Dementia, Dominantly inherited sensory neuropathy, Dysarthria, Graves disease, Hearing impairment, Hearing loss, Hereditary sensory and autonomic neuropathy, Hypertension, Medulloblastoma, Mood disorder, Myelodysplastic syndrome, Otosclerosis, Pituitary stalk interruption syndrome, Prostatic intraepithelial neoplasia, Prostatic neoplasms, Schizophrenia, Sensory neuropathy, Spastic ataxia, Stomach neoplasmsView all (24 more) |
420
|
|
|
DNA methyltransferase 3 alpha |
DNMT3A2, HESJAS, M.HsaIIIA, TBRS |
Ankylosing spondylitis, Atrial fibrillation, Autism, Biliary cirrhosis, Breast cancer, Breast neoplasms, Obstructive pulmonary disease, Renal cell carcinoma, Clonal cytopenia of undetermined significance, Congenital neurologic anomalies, Craniofacial abnormalities, Crohn disease, Melanoma, Desbuquois syndrome, Microcephalic dwarfism, Dwarfism, Global developmental delay, Growth disorder, Hypertension, Inflammatory bowel disease, Intellectual developmental disorder, Leukemia, Myeloid leukemia, Promyelocytic leukemia, Lung neoplasms, Metabolic syndrome, Microcephaly, Multiple sclerosis, Myelodysplastic syndrome, Myeloproliferative disorder, Neurodevelopmental disorder, Obesity, Osteoarthritis, Polycythemia vera, Biliary cholangitis, Psoriasis, Sclerosing cholangitis, Sezary syndrome, Specific learning disability, Diabetes mellitus type 2, Ulcerative colitis, Uterine fibroidView all (27 more) |
