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"
451 to 460 of 596 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

451
Dolichyl-phosphate N-acetylglucosaminephosphotransferase 1
ALG7, CDG-Ij, CDG1J, CMS13, CMSTA2, D11S366, DGPT, DPAGT, DPAGT2, G1PT, GPT, UAGT, UGAT
Colorectal neoplasms, Congenital disorder of glycosylation, Congenital myasthenic syndrome, Myasthenic syndrome, Stomach neoplasms, Tubular aggregate myopathy

452
Deleted in primary ciliary dyskinesia homolog (mouse)
-
Desbuquois syndrome, Insomnia

453
Dipeptidase 1
MBD1, MDP, RDP
Biliary tract cancer, Breast cancer, Cancer, Cardiovascular disease, Cervical cancer, Kidney disease, Ulcerative colitis, Colorectal cancer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Hypertension, Hyperuricemia
View all (11 more)

454
Double PHD fingers 1
BAF45b, NEUD4, SMARCG1, neuro-d4
Prostate cancer

455
Double PHD fingers 2
CSS7, REQ, SMARCG2, UBID4, ubi-d4
Coffin-siris syndrome, Desbuquois syndrome, Gout, Osteoarthritis

456
Double PHD fingers 3
BAF45C, CERD4, SMARCG3
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Kidney disease, Obstructive pulmonary disease, Clear cell renal cell carcinoma, Gout, Kidney cancer, Major depressive disorder, Metabolic syndrome, Scoliosis, Systemic lupus erythematosus, Diabetes mellitus type 2

457
Diphthamide biosynthesis 1
DEDSSH, DPH2L, DPH2L1, OVCA1
Asthma, Craniofacial dysplasia short stature ectodermal anomalies intellectual disability syndrome, Dandy-walker syndrome, Developmental delay with short stature and dysmorphic facial features, Global developmental delay, Hydrocephalus, Intracerebral hemorrhage

458
Diphthamide biosynthesis 2
DEDSSH2, DPH2L2
Craniofacial dysplasia short stature ectodermal anomalies intellectual disability syndrome, Developmental delay with short stature and dysmorphic facial features, Global developmental delay, Intellectual developmental disorder, Schizophrenia, Ventricular septal defect

459
Diphthamide biosynthesis 5
AD-018, CGI-30, HSPC143, NEDSFF, NPD015
Crohn disease, Inflammatory bowel disease, Neurodevelopmental disorder, Ulcerative colitis

460
Diphthamine biosynthesis 6
ATPBD4
Metabolic syndrome, Diabetes mellitus type 2