Gene: DES ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1674
Gene Symbol: DES
DES 		0.330 Biomarker disease BEFREE Some cases of familial dilated cardiomyopathy show gene abnormalities for cytoskeletal components such as desmin and laminin A/C. 12469210 2003
Entrez Id: 1674
Gene Symbol: DES
DES 		0.330 GeneticVariation disease BEFREE To date, two genes for X-linked FDCM (dystrophin, G4.5) have been identified and four genes for the autosomal dominant form (actin, desmin, lamin A/C, delta-sarcoglycan) have been described. 11899244 2001
Entrez Id: 1674
Gene Symbol: DES
DES 		0.330 GeneticVariation disease BEFREE To date, 2 genes for X-linked familial dilated cardiomyopathy (dystrophin, G4.5) have been identified and 4 genes for the autosomal dominant form (actin, desmin, lamin A/C, delta-sarcoglycan) have been described. 11781950 2001
Entrez Id: 1674
Gene Symbol: DES
DES 		0.330 GermlineCausalMutation disease ORPHANET Desmin mutation responsible for idiopathic dilated cardiomyopathy. 10430757 1999