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APBA2

Gene

amyloid beta precursor protein binding family A member 2

HGNCHGNC:579EnsemblENSG00000034053NCBI Gene321
Locus: gene with protein productLocation: 15q13.1

Also known as

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

Also known asX11L · MINT2 · D15S1518E · LIN-10 · MGC:14091 · HsT16821
View full nomenclature history (9)
Previous symbolsX11L, MINT2
Alias symbolsD15S1518E, LIN-10, MGC:14091, HsT16821
Previous namesamyloid beta (A4) precursor protein-binding, family A, member 2 (X11-like), X11-like, amyloid beta (A4) precursor protein-binding, family A, member 2

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.

Hair color
Alcohol drinking
Uveitis
Parasitic Diseases
Stroke
Diabetes Mellitus
Urolithiasis

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.

PDZ domain containing

Provenance

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