Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1674
Gene Symbol: DES
DES 		0.900 Biomarker disease GENOMICS_ENGLAND Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia. 29212896 2018
Entrez Id: 1674
Gene Symbol: DES
DES 		0.900 Biomarker disease GENOMICS_ENGLAND Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257 2017
Entrez Id: 1674
Gene Symbol: DES
DES 		0.900 GeneticVariation disease UNIPROT Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect. 26724190 2016
Entrez Id: 1674
Gene Symbol: DES
DES 		0.900 GeneticVariation disease UNIPROT The novel desmin mutant p.A120D impairs filament formation, prevents intercalated disk localization, and causes sudden cardiac death. 24200904 2013
Entrez Id: 1674
Gene Symbol: DES
DES 		0.900 Biomarker disease GENOMICS_ENGLAND The genetics of dilated cardiomyopathy. 20186049 2010
Entrez Id: 1674
Gene Symbol: DES
DES 		0.900 Biomarker disease MGD The absence of desmin leads to cardiomyocyte hypertrophy and cardiac dilation with compromised systolic function. 10591032 1999
Entrez Id: 1674
Gene Symbol: DES
DES 		0.900 GeneticVariation disease UNIPROT Desmin mutation responsible for idiopathic dilated cardiomyopathy. 10430757 1999
Entrez Id: 1674
Gene Symbol: DES
DES 		0.900 Biomarker disease MGD Disruption of muscle architecture and myocardial degeneration in mice lacking desmin. 8794866 1996
Entrez Id: 1674
Gene Symbol: DES
DES 		0.900 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 1674
Gene Symbol: DES
DES 		0.900 Biomarker disease CTD_human
Entrez Id: 1674
Gene Symbol: DES
DES 		0.900 CausalMutation disease CLINVAR