ABI2

Gene

abl interactor 2

HGNCHGNC:24011 EnsemblENSG00000138443 NCBI Gene10152

Locus: gene with protein productLocation: 2q33.2

Also known as

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

Also known asABI-2 · AIP-1 · ABI2B · AblBP3 · argBPIA · SSH3BP2

View full nomenclature history (7)

Alias symbolsABI-2, AIP-1, ABI2B, AblBP3, argBPIA, SSH3BP2

Previous namesabl-interactor 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.

Neurodegenerative Diseases

Wounds and Injuries

Neurodevelopmental Disorders

Hypothyroidism

Neoplasms

Carcinoma, Hepatocellular

Genetic central nervous system malformation

Nasopharyngeal Carcinoma

Myelodysplastic syndrome

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.

SCAR/WAVE complexABI family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.

Open TargetsGene–disease associations from the Open Targets Platform.