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ITGA11

Gene

integrin subunit alpha 11

HGNCHGNC:6136EnsemblENSG00000137809NCBI Gene22801
Locus: gene with protein productLocation: 15q23

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asHsT18964
View full nomenclature history (2)
Alias symbolsHsT18964
Previous namesintegrin, alpha 11

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Dupuytren Contracture
Keloid
Self-injurious ideation
Diabetes Mellitus, Type 2
Glaucoma

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Integrin alpha subunits

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.