ATOSB

Gene

atos homolog B

HGNCHGNC:25666 EnsemblENSG00000005238 NCBI Gene80256

Locus: gene with protein productLocation: 9p13.3

Also known as

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

Also known asFAM214B · FLJ11560 · bA182N22.6

View full nomenclature history (6)

Previous symbolsFAM214B

Alias symbolsFLJ11560, bA182N22.6

Previous namesKIAA1539, family with sequence similarity 214, member B, family with sequence similarity 214 member B

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

Autosomal dominant macrothrombocytopenia

Leukemia, Erythroblastic, Acute

Rare hemorrhagic disorder due to a constitutional platelet anomaly

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.

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.