MS4A8

Gene

membrane spanning 4-domains A8

HGNCHGNC:13380 EnsemblENSG00000166959 NCBI Gene83661

Locus: gene with protein productLocation: 11q12.2

Also known as

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

Also known asMS4A8B · MS4A4 · CD20L5

View full nomenclature history (5)

Previous symbolsMS4A8B

Alias symbolsMS4A4, CD20L5

Previous namesmembrane-spanning 4-domains, subfamily A, member 8B, membrane-spanning 4-domains, subfamily A, member 8

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.

Carbohydrate Metabolism, Inborn Errors

Paroxysmal tachycardia

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.

Membrane spanning 4-domains

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.