Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "D"
361 to 370 of 466 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

361
Dipeptidase 3
MBD3

362
DnaJ heat shock protein family (Hsp40) member C1
DNAJL1, ERdj1, HTJ1, MTJ1
Asthma, Attention deficit hyperactivity disorder, Breast cancer, Cancer, Central nervous system cancer, Colorectal cancer, Endometriosis, Hypertension, Estrogen-receptor negative breast cancer, Glioblastoma, Glioma, Insomnia, Lung cancer, Melanoma, Ovarian cancer
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363
Dynein axonemal heavy chain 10 opposite strand
-

364
DNA cross-link repair 1C
A-SCID, DCLREC1C, RS-SCID, SCIDA, SNM1C
Common variable immunodeficiency, Ehlers-danlos syndrome, Migraine, Omenn syndrome, Severe combined immunodeficiency

365
Dynein axonemal intermediate chain 2
CILD9, DIC2, oda6
Alzheimer disease, Autism, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Dementia, Major depressive disorder

366
DEP domain containing MTOR interacting protein
DEP.6, DEPDC6, hDEPTOR
Alzheimer disease, Human immunodeficiency virus infection, Idiopathic pulmonary fibrosis, Interstitial lung disease, Oligodendroglioma, Scoliosis

367
DNA cross-link repair 1B
APOLLO, DKCB8, SNM1B, SNMIB
Breast cancer, Cardiovascular disease, Coronary artery disease, Melanoma, Dyskeratosis congenita, Fanconi anemia, Hoyeraal hreidarsson syndrome, Myocardial infarction, Non-melanoma skin carcinoma, Rheumatoid arthritis, Spastic paraplegia, Hereditary spastic paraplegia, Diabetes mellitus, type 1

368
Double homeobox 4 like 5 (pseudogene)
-

369
DDRGK domain containing 1
C20orf116, SEMDSH, UFBP1, dJ1187M17.3
Hepatitis c virus infection, Desbuquois syndrome, Parkinson disease, Spondyloepimetaphyseal dysplasia

370
Dystonin
BP240, BPA, BPAG1, CATX-15, CATX15, D6S1101, DMH, DT, EBS3, EBSB2, HSAN6, MACF2
Alzheimer disease, Atrial fibrillation, Autism, Cardiomyopathy, Charcot-marie-tooth disease, Distal spinal muscular atrophy, Epidermolysis bullosa, Esophageal atresia, Global developmental delay, Gout, Hereditary sensory and autonomic neuropathy, Moyamoya angiopathy, Multiple sclerosis, Open angle glaucoma, Pancreatic cancer
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