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ITGA7

integrin subunit alpha 7

HCNC Approved Symbol
ITGA7 (HGNC:6143)
Genomic Coordinates
12:55,684,568 - 55,716,400 (12q13.2)
Synonyms
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Muscular dystrophy, congenital, due to ITGA7 deficiency
613204AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the ITGA7 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results