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161
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|
|
Dynein cytoplasmic 1 heavy chain 1 |
CDCBM13, CMT2O, DHC1, DHC1a, DNCH1, DNCL, DNECL, DYHC, Dnchc1, HL-3, SMALED1, p22 |
Amyotrophic lateral sclerosis, Arthrogryposis multiplex congenita, Autism, Cerebellar ataxia, Charcot-marie-tooth disease, Childhood-onset spinal muscular atrophy, Distal hereditary motor neuropathy, Nonsyndromic intellectual disability, Cerebellar atrophy, Congenital neurologic anomalies , Cortical dysplasia with other brain malformations, Dejerine-sottas disease, Distal spinal muscular atrophy, Global developmental delay, Gross motor development delay, Motor neuron disease, Hypertrophic neuropathy, Intellectual developmental disorder, Lissencephaly, Macrogyria, Cortical development malformation, Microcephaly, Myopathy, Neurodevelopmental disorders, Neuronopathy, distal hereditary motor, Pena-shokeir syndrome type i, Peripheral neuropathy, Peroneal muscle atrophy, Polymicrogyria, Polyneuropathy, Rhizomelic chondrodysplasia punctata, Roussy-levy syndrome, Saldino-noonan syndrome, Seizures, Spinal muscular atrophy, Papillary thyroid cancer, Tonic-clonic epilepsyView all (22 more) |
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162
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|
|
Dynein cytoplasmic 1 intermediate chain 1 |
DNCI1, DNCIC1 |
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163
|
|
|
Dynein cytoplasmic 1 intermediate chain 2 |
DIC74, DNCI2, IC2, NEDMIBA |
|
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164
|
|
|
Dynamin 2 |
CMT2M, CMTDI1, CMTDIB, DI-CMTB, DYN2, DYNII, LCCS5 |
Centronuclear myopathy, Charcot-marie-tooth disease, Obstructive pulmonary disease, Hyperlipidemia, Irritable bowel syndrome, Lethal congenital contracture syndrome, Moyamoya angiopathy, Myocardial infarction, Myofibrillar myopathy, Myopathy, Peripheral neuropathy, Psoriasis, Hereditary spastic paraplegia, Stroke, Ventricular dysfunction, X-linked centronuclear myopathyView all (1 more) |
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165
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|
|
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 neoplasm, Carcinoma, Pancreatic carcinoma, Cardiovascular disease, Cerebellar ataxia, Cerebellar ataxia, deafness, and narcolepsy, Cerebellar atrophy, Cerebral atrophy, Charcot-marie-tooth disease, Chorea, Colonic neoplasm, Deglutition disorder, Dementia, Dysarthria, Graves disease, Hearing impairment, Hearing loss, Hereditary sensory and autonomic neuropathy, Hypertension, Medulloblastoma, Mood disorder, Myelodysplastic syndrome, Hereditary sensory neuropathy, Otosclerosis, Pituitary stalk interruption syndrome, Prostatic intraepithelial neoplasia, Prostatic neoplasm, Schizophrenia, Sensory neuropathy, Spastic ataxia, Stomach neoplasmsView all (23 more) |
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166
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|
|
DNA methyltransferase 3 alpha |
DNMT3A2, HESJAS, M.HsaIIIA, TBRS |
Ankylosing spondylitis, Atrial fibrillation, Autism, Biliary cirrhosis, Breast cancer, Breast neoplasm, Obstructive pulmonary disease, Congenital neurologic anomalies , Craniofacial abnormalities, Crohn disease, Melanoma, Desbuquois syndrome, Global developmental delay, Growth disorder, Hypertension, Inflammatory bowel disease, Intellectual developmental disorder, Lethal congenital contracture syndrome, Myeloid leukemia, Promyelocytic leukemia, Lung neoplasms, Metabolic syndrome, Microcephaly, Multiple sclerosis, Myelodysplastic syndrome, Myeloproliferative disorder, Neurodevelopmental disorders, Obesity, Osteoarthritis, Polycythemia vera, Biliary cholangitis, Psoriasis, Sclerosing cholangitis, Sezary syndrome, Specific learning disability, Diabetes mellitus, type 2, Ulcerative colitis, Uterine fibroidView all (23 more) |
|
167
|
|
|
DNA methyltransferase 3 beta |
FSHD4, ICF, ICF1, M.HsaIIIB |
Androgenetic alopecia, Ankylosing spondylitis, Attention deficit hyperactivity disorder, Autism, Breast neoplasm, Carcinoma, Craniofacial abnormalities, Crohn disease, Dyslexia, Schizophrenia, Facioscapulohumeral muscular dystrophy, Immunodeficiency-centromeric instability-facial anomalies syndrome, Female infertility, Inflammatory bowel disease, Kabuki syndrome, Mood disorder, Myelodysplastic syndrome, Non-melanoma skin carcinoma, Prostate cancer, Prostatic neoplasm, Psoriasis, Rheumatoid arthritis, Sclerosing cholangitis, Stomach neoplasms, Ulcerative colitisView all (10 more) |
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168
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|
|
Dedicator of cytokinesis 1 |
DOCK180, ced5 |
Alzheimer disease, Amyotrophic lateral sclerosis, Astrocytoma, Breast cancer, Cardiomyopathy, Duchenne muscular dystrophy, Insomnia, Lung cancer, Metabolic syndrome, Moyamoya disease, Oligodendroglioma, Prostate cancer, Schizophrenia, Scoliosis, Diabetes mellitus, type 2 |
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169
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|
|
Dedicator of cytokinesis 2 |
IMD40 |
Astrocytoma, Bipolar disorder, Breast cancer, Central nervous system cancer, Combined immunodeficiency disease, Coronary aneurysm, Dementia, Digestive system disease, Glioma, Immunodeficiency, Inflammatory bowel disease, Neuroblastoma, Prostate cancer, Scoliosis, Triple-negative breast cancer, Ulcerative colitisView all (1 more) |
|
170
|
|
|
Dedicator of cytokinesis 3 |
MOCA, NEDIDHA, PBP |
Alzheimer disease, Asthma, Attention deficit hyperactivity disorder, Breast cancer, Cholangiocarcinoma, Colorectal cancer, Diverticular disease, Global developmental delay, Gout, Insomnia, Major depressive disorder, Melanoma, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Prostate cancer, Respiratory system disease, Schizophrenia, Sclerosing cholangitis, Hypertension, Diabetes mellitus, type 2View all (5 more) |