Gene
itga7
- ID
- ZDB-GENE-070501-10
- Name
- integrin, alpha 7
- Symbol
- itga7 Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 11 Mapping Details/Browsers
- Description
- Involved in cell-matrix adhesion; muscle attachment; and skeletal muscle tissue development. Human ortholog(s) of this gene implicated in Duchenne muscular dystrophy; congenital muscular dystrophy due to integrin alpha-7 deficiency; and muscular disease. Is expressed in myoseptum; myotome; skeletal muscle cell; and somite. Orthologous to human ITGA7 (integrin subunit alpha 7).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 5 figures from 4 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| congenital muscular dystrophy due to integrin alpha-7 deficiency | Alliance | Muscular dystrophy, congenital, due to ITGA7 deficiency | 613204 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available