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COVID-19 research

Gene: DMD

Red List (low evidence)

DMD (dystrophin)
EnsemblGeneIds (GRCh38): ENSG00000198947
EnsemblGeneIds (GRCh37): ENSG00000198947
OMIM: 300377, Gene2Phenotype
DMD is in 20 panels

1 review

Sarah Leigh (Genomics England Curator)

Red List (low evidence)

A dystrophin-deficient mouse model was predisposed to enterovirus-induced cardiomyopathy, with more severe cardiomyopathy, advancing, with increased viral replication than in infected wildtype mice.
Created: 4 May 2020, 3:17 p.m. | Last Modified: 4 May 2020, 3:17 p.m.
Panel Version: 0.176

Mode of inheritance
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)

Publications

History Filter Activity

2 Jun 2020, Gel status: 1

Added Tag

Sarah Leigh (Genomics England Curator)

Tag Skewed X-inactivation tag was added to gene: DMD.

21 Apr 2020, Gel status: 1

Created, Added New Source, Set mode of inheritance

Sarah Leigh (Genomics England Curator)

gene: DMD was added gene: DMD was added to Viral susceptibility. Sources: OMIM Mode of inheritance for gene: DMD was set to