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TAGAP

Gene

T cell activation RhoGTPase activating protein

HGNCHGNC:15669EnsemblENSG00000164691NCBI Gene117289
Locus: gene with protein productLocation: 6q25.3

Also known as

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

Also known asIDDM21 · FLJ32631 · ARHGAP47
View full nomenclature history (5)
Alias symbolsIDDM21, FLJ32631, ARHGAP47
Previous namesT-cell activation GTPase activating protein, T-cell activation RhoGTPase activating protein

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.

Psoriasis
Celiac Disease
Hypothyroidism
Crohn's Disease
Arthritis, Rheumatoid
Dermatitis
Multiple Sclerosis
Dermatitis, Atopic
Skin Diseases
Psoriasis vulgaris

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.

Rho GTPase activating proteins

Provenance

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