FHIP2A

Gene

FHF complex subunit HOOK interacting protein 2A

HGNCHGNC:29320 EnsemblENSG00000151553 NCBI Gene57700

Locus: gene with protein productLocation: 10q25.3

Also known as

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

Also known asFAM160B1 · bA106M7.3

View full nomenclature history (4)

Previous symbolsFAM160B1

Alias symbolsbA106M7.3

Previous namesKIAA1600, family with sequence similarity 160 member B1

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.

Arthritis

Retinitis Pigmentosa

Leber Congenital Amaurosis

Cone rod dystrophy

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.

Armadillo like helical domain containingFHF complex

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.