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GeneQ18028020· pop 6· linked from 41 articles

Also 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 (−)
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].

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
View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Show 5 more facts
HomoloGene ID
37592
genomic end
55716404
genomic start
56078352
cytogenetic location
12q13.2
Sources (8)

via Wikidata · CC0

Available in 6 languages

via Wikidata sitelinks · CC0

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