Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3281 to 3290 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3281
Cysteine and tyrosine rich 1
C21orf95
Alzheimer disease, Color vision deficiency, Dementia, Prostate cancer, Scoliosis

3282
CXXC motif containing zinc binding protein
C1orf123
Carnitine palmitoyltransferase deficiency

3283
D-2-hydroxyglutarate dehydrogenase
D2HGD
Amino acid metabolism disorder, Asthma, Eczema, Obstructive pulmonary disease, Combined d-2- and l-2-hydroxyglutaric aciduria, D-2-hydroxyglutaric aciduria, Glioma, Mitochondrial disease, Respiratory system disease, Seasonal allergic rhinitis

3284
Dishevelled associated activator of morphogenesis 1
-
Major depressive disorder, Diabetes mellitus type 2

3285
Dishevelled associated activator of morphogenesis 2
NPHS24, dJ90A20A.1
Aortic atherosclerosis, Kidney disease, Combined molybdoflavoprotein enzyme deficiency, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Hypospadias, Nephrotic syndrome, Kidney failure, Oligodendroglioma, Osteoporosis, Schizophrenia, Scoliosis, Diabetes mellitus type 2

3286
DAB adaptor protein 1
SCA37
Alzheimer disease, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Breast cancer, Bulimia, Clonal hematopoiesis, Color vision deficiency, Colorectal adenoma, Coronary artery disease, Hoarding disorder, Insomnia, Intracerebral hemorrhage, Metabolic syndrome, Kawasaki disease
View all (8 more)

3287
DAB adaptor protein 2
DOC-2, DOC2
Kidney disease, Diverticular disease, Gout, Pancreatic cancer, Systemic lupus erythematosus

3288
DAB2 interacting protein
AF9Q34, AIP-1, AIP1, DIP1/2
Aneurysm, Aortic aneurysm, Arterial occlusive disease, Bone disease, Cartilage disease, Central nervous system cancer, Ischemic heart disease, Coronary artery disease, Glioblastoma, Glioma, Keratoconus, Lung neoplasms, Myocardial infarction, Myocardial ischemia, Periodontitis
View all (3 more)

3289
Dachshund family transcription factor 1
DACH
Alzheimer disease, Anophthalmia/microphthalmia-esophageal atresia syndrome, Attention deficit hyperactivity disorder, Kidney disease, Congenital left-sided heart lesions, Gout, Spondylosis, Amyotrophic lateral sclerosis, Substance abuse

3290
Dachshund family transcription factor 2
-
Alzheimer disease, Scoliosis