Genes | GeDiPNet - Gene Disease Pathway & Associations

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3731 to 3740 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
3731	84444	DOT1L	DOT1 like histone lysine methyltransferase	DOT1, KMT4, NDNS	Aneurysm, Aortic aneurysm, Atrial fibrillation, Breast cancer, Obstructive pulmonary disease, Colorectal neoplasms, Developmental disability, Estrogen-receptor negative breast cancer, Osteoarthritis, Prostatic neoplasms, Systemic lupus erythematosus
3732	1798	DPAGT1	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
3733	25911	DPCD	Deleted in primary ciliary dyskinesia homolog (mouse)	-	Desbuquois syndrome, Insomnia
3734	1800	DPEP1	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)
3735	8193	DPF1	Double PHD fingers 1	BAF45b, NEUD4, SMARCG1, neuro-d4	Prostate cancer
3736	5977	DPF2	Double PHD fingers 2	CSS7, REQ, SMARCG2, UBID4, ubi-d4	Coffin-siris syndrome, Desbuquois syndrome, Gout, Osteoarthritis
3737	8110	DPF3	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
3738	1801	DPH1	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
3739	1802	DPH2	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
3740	51611	DPH5	Diphthamide biosynthesis 5	AD-018, CGI-30, HSPC143, NEDSFF, NPD015	Crohn disease, Inflammatory bowel disease, Neurodevelopmental disorder, Ulcerative colitis

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