ITGA7
Sign in to saveAlso known as integrin subunit alpha 7
protein-coding gene in the species Homo sapiens
Gene data
ITGA7- Name
- integrin subunit alpha 7
- Type
- protein-coding
- Position
- 55,684,568–55,716,404 (−)
- Ensembl
- ENSG00000135424
- RefSeq RNA
- NM_001144996.2, NM_001144997.2, NM_001367993.1, NM_001367994.1, NM_001374465.1
- RefSeq protein
- NP_001138468.1, NP_001138469.1, NP_001354922.1, NP_001354923.1, NP_001361394.1
The protein encoded by this gene belongs to the integrin alpha chain family. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. They mediate a wide spectrum of cell-cell and cell-matrix interactions, and thus play a role in cell migration, morphologic development, differentiation, and metastasis. This protein functions as a receptor for the basement membrane protein laminin-1. It is mainly expressed in skeletal and cardiac muscles and may be involved in differentiation and migration processes during myogenesis. Defects in this gene are associated with congenital myopathy. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Feb 2009].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
integrin subunit alpha 7
- Symbol
- ITGA7
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 12:55,679,139-55,716,404
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 37592
- exact match
- identifiers.org/ncbigene/3679
- genomic end
- 55716404
- genomic start
- 56078352
- cytogenetic location
- 12q13.2
Sources (8)
via Wikidata · CC0