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ACSM2B

Gene

acyl-CoA synthetase medium chain family member 2B

HGNCHGNC:30931EnsemblENSG00000066813NCBI Gene348158
Locus: gene with protein productLocation: 16p12.3

Also known as

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

Also known asACSM2 · HXMA · HYST1046
View full nomenclature history (5)
Previous symbolsACSM2
Alias symbolsHXMA, HYST1046
Previous namesacyl-CoA synthetase medium-chain family member 2
Alias namesxenobiotic/medium chain fatty acid:CoA ligase

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.

Bipolar Disorder
Neoplasms
Kidney Failure, Chronic
Renal Insufficiency
Autosomal dominant primary hypomagnesemia with hypocalciuria

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.

Acyl-CoA synthetase family

Provenance

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