MYH3
HGNC:7573 · SaudiVarKB evidence summary derived from retained literature mentions.
3Gene mentions
3Publications
0Linked variants
1Associated phenotypes
Associated phenotypes
Co-mentioned in MYH3 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| Duchenne muscular dystrophy | — | 2 | 2 |
Linked variants
Variants normalized to MYH3| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Not specified | — | 29 | 1 |
Supporting publications
3 records- 2025Decoding Myosin-3 mutational hotspots: Linking deleterious variants to Duchenne muscular dystrophy severity and psychiatric comorbidities.PloS onePubMed ↗
- 2024Discovering Promising Biomarkers and Therapeutic Targets for Duchenne Muscular Dystrophy: a Multiomics Meta-Analysis Approach.Molecular neurobiologyPubMed ↗
- 2012Grouping patients for masseter muscle genotype-phenotype studies.The Angle orthodontistPubMed ↗