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DMD
Genedystrophin
Encodes
The protein product this gene encodes, reached through the canonical GENE→PROTEIN (encodes) relation. Its biology, drugs, indications, trials and therapeutic evidence live on the protein's own page.
Also known as
Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.
MRX85 · BMD · DXS142 · DXS164 · DXS206 · DXS230 · DXS239 · DXS268 · DXS269 · DXS270 · DXS272
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MRX85
BMD, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272
mental retardation, X-linked 85, dystrophin (muscular dystrophy, Duchenne and Becker types), includes DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272
muscular dystrophy, Duchenne and Becker types
Associated diseases
Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.
Gene family
HGNC gene-group membership.
Zinc fingers ZZ-typeMicroRNA protein coding host genesSpectrin repeat containing
Provenance
HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.