LILRA2

Gene

leukocyte immunoglobulin like receptor A2

HGNCHGNC:6603 EnsemblENSG00000239998 NCBI Gene11027

Locus: gene with protein productLocation: 19q13.42

Also known as

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

Also known asLIR-7 · ILT1 · CD85h · LIR7

View full nomenclature history (6)

Alias symbolsLIR-7, ILT1, CD85h, LIR7

Previous namesleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 2

Alias namesleucocyte Ig-like receptor A2

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.

Metabolic Syndrome

Familial focal epilepsy with variable foci

Genetic central nervous system malformation

lissencephaly due to TUBA1A mutation

Exocrine pancreatic carcinoma

Lupus Erythematosus, Systemic

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.

CD moleculesActivating leukocyte immunoglobulin like receptors

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.