Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
2761 to 2770 of 12229 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2761
Atrophin 1
B37, CHEDDA, D12S755E, DRPLA, HRS, NOD
Action myoclonus-renal failure syndrome, Blepharospasm, Cardiovascular abnormalities, Central visual impairment, Cerebellar ataxia, Cerebral atrophy, Choreoathetosis, Congenital epicanthus, Cryptorchidism, Dementia, Dentatorubral pallidoluysian atrophy, Developmental delay, Dysarthria, Dysphagia, Gastroesophageal reflux disease
View all (14 more)

2762
Desmocollin 1
CDHF1, DG2/DG3
Melanoma

2763
Desmocollin 2
ARVD11, CDHF2, DG2, DGII/III, DSC3
Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular cardiomyopathy with or without mild palmoplantar keratoderma, Arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair, Cardiomyopathy, Palmoplantar keratoderma, Ventricular arrhythmia, Ventricular cardiomyopathy

2764
Desmocollin 3
CDHF3, DSC, DSC1, DSC2, DSC4, HT-CP
Breast cancer, Mammary neoplasms, Breast carcinoma, Hereditary hypotrichosis with skin vesicles, Hypotrichosis, Hypotrichosis and recurrent skin vesicles, Marfan syndrome

2765
DS cell adhesion molecule
CHD2, CHD2-42, CHD2-52
Anxiety disorder, Bipolar disorder, Charcot-marie-tooth disease, Dysmorphic features, Hirschsprung disease, Intracranial aneurysm, Kidney failure, Mental depression, Neurodevelopmental disorders

2766
Regulator of calcineurin 1
ADAPT78, CSP1, DSC1, DSCR1, MCIP1, RCN1
Akinetic-rigid variant of huntington disease, Congenital heart defects, Down syndrome, Huntington disease, Liver carcinoma, Malignant neoplasm, Rheumatoid arthritis, Trisomy 21

2767
Desmoglein 1
CDHF4, DG1, DSG, EPKHE, EPKHIA, PPKS1, SPPK1
Bicuspid aortic valve, Dermatitis, Dermatitis-multiple allergies-metabolic wasting syndrome, Diffuse palmoplantar hyperkeratosis, Diffuse palmoplantar keratoderma with painful fissures, Exfoliative dermatitis, Focal palmoplantar keratoderma with joint keratoses, Hypotrichosis, Keratosis palmoplantaris striata, Metabolic diseases, Palmoplantar keratoderma, Palmoplantar keratosis, Psoriasiform eczema, Striate palmoplantar keratoderma

2768
Desmoglein 2
CDHF5, HDGC
Alzheimer disease, Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hearing loss, Hypertrophic cardiomyopathy, Lipoatrophy, Lipodystrophy, Myopathy, Palmoplantar keratoderma, Ventricular cardiomyopathy, Ventricular tachycardia

2769
Angiotensinogen
ANHU, SERPINA8, hFLT1
Allanson pantzar mcleod syndrome, Alveolitis, Anemia, Aortic aneurysm, Aortic dissection, Atherosclerosis, Bipolar disorder, Bright disease, Cardiomyopathy, Cardiovascular abnormalities, Cardiovascular diseases, Carotid artery disease, Carotid atherosclerosis, Catalepsy, Cholestasis
View all (39 more)

2770
TSC22 domain family member 3
DIP, DSIPI, GILZ, TSC-22R
Compensatory hyperinsulinemia, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Hyperinsulinism, Testicular diseases