Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "D"
481 to 490 of 596 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

481
Dihydropyrimidinase like 2
CRMP-2, CRMP2, DHPRP2, DRP-2, DRP2, N2A3, ULIP-2, ULIP2
Alzheimer disease, Atrial fibrillation, Nonsyndromic intellectual disability, Barrett esophagus, Bipolar disorder, Cardiovascular disease, Paranoid schizophrenia, Major depressive disorder, Esophageal adenocarcinoma, Oligodendroglioma, Osteoarthritis, Schizophrenia

482
Dihydropyrimidinase like 3
CRMP-4, CRMP4, DRP-3, DRP3, LCRMP, ULIP, ULIP-1
Autism, Scoliosis, Squamous cell carcinoma

483
Dihydropyrimidinase like 5
CRAM, CRMP-5, CRMP5, CV2, RTSC4, Ulip6
Dandy-walker syndrome, Diabetic neuropathy, Gout, Non-specific syndromic intellectual disability, Obesity, Osteoarthritis, Prostate cancer, Ritscher-schinzler syndrome, Diabetic nephropathy, Venous thromboembolism

484
DEAQ-box RNA dependent ATPase 1
-
Arthrogryposis multiplex congenita, Pena-shokeir syndrome

485
Down-regulator of transcription 1
NC2, NC2-BETA, NC2B, NCB2
Crohn disease, Gout, Inflammatory bowel disease, Metabolic syndrome, Diabetes mellitus type 2, Ulcerative colitis

486
DNA damage regulated autophagy modulator 1
DRAM
Brain aneurysm, Liver cirrhosis, Scoliosis, Systemic lupus erythematosus

487
DNA damage regulated autophagy modulator 2
CORD21, PRO180, TMEM77, WWFQ154
Color vision deficiency, Cone-rod dystrophy, Retinitis pigmentosa

488
DR1 associated protein 1
NC2-alpha
Breast cancer, Gout, Melanoma, Multiple sclerosis, Open angle glaucoma

489
Dorsal inhibitory axon guidance protein
AGPA3119, C1orf187, UNQ3119, neucrin
Alzheimer disease, Autism, Obsessive-compulsive disorder, Parkinson disease, Schizophrenia

490
Dynein regulatory complex subunit 1
C2orf39, CCDC164, CILD21, SPGF80
Ciliary dyskinesia, with or without situs inversus, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Congenital impairment of spermatozoa motility, Polynesian bronchiectasis, Spermatogenic failure