Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3801 to 3810 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3801
Destrin, actin depolymerizing factor
ACTDP, ADF, HEL32, bA462D18.2
Congestive heart failure, Heart failure, Migraine, Ventricular remodeling

3802
DSTN pseudogene 4
-
Iga nephropathy, Venous thromboembolism

3803
Dual serine/threonine and tyrosine protein kinase
CAKUT1, DustyPK, HDCMD38P, RHDNS1, RIP5, RIPK5, SPG23
Spastic paraplegia, Basal cell carcinoma, Kidney disease, Obstructive pulmonary disease, Colorectal cancer, Hereditary spastic paraplegia, Congenital anomalies of kidney and urinary tract, Coronary artery disease, Melanoma, Dupuytren contracture, Metabolic syndrome, Obesity, Diabetes mellitus type 2

3804
D-aminoacyl-tRNA deacylase 1
C20orf88, DTD, DUE-B, DUEB, HARS2, pqn-68
Dry eye syndrome, Diabetes mellitus type 2

3805
Death domain containing 1
-
Obstructive pulmonary disease, Leber congenital amaurosis, Muscular dystrophy, Optic atrophy, Retinitis pigmentosa

3806
Denticleless E3 ubiquitin protein ligase adapter
CDT2, DCAF2, L2DTL, RAMP
Adenoid cystic carcinoma, Hepatocellular carcinoma, Large artery stroke, Salivary gland neoplasms

3807
Dystrobrevin alpha
D18S892E, DRP3, DTN, DTN-A, LVNC1, MMCKR2
Astrocytoma, Atrial fibrillation, Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy, Central nervous system cancer, Color vision deficiency, Congenital heart disease, Generalized anxiety disorder, Glioblastoma, Glioma, Hypertrophic cardiomyopathy, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Meniere disease
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3808
Dystrobrevin beta
-
Alzheimer disease, Lymphocytic leukemia, Crohn disease, Melanoma, Hodgkin lymphoma, Inflammatory bowel disease, Lung cancer, Multiple myeloma, Diabetes mellitus type 2

3809
Dystrobrevin binding protein 1
BLOC1S8, DBND, HPS7, My031, SDY
Basal cell carcinoma, Bipolar disorder, Corneal astigmatism, Major depressive disorder, Hermansky-pudlak syndrome, Interstitial lung disease, Mood disorder, Non-small cell lung carcinoma, Schizophrenia, Scoliosis, Sensory peripheral neuropathy, Depression, Squamous cell carcinoma, Vascular dementia

3810
DTW motif tRNA-uridine aminocarboxypropyltransferase 1
MDS009
Bone fracture, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Inflammatory bowel disease, Lung cancer, Metabolic syndrome, Non-melanoma skin carcinoma, Oral cavity carcinoma, Scoliosis, Squamous cell carcinoma