CHMP2B

Gene

charged multivesicular body protein 2B

HGNCHGNC:24537 EnsemblENSG00000083937 NCBI Gene25978

Locus: gene with protein productLocation: 3p11.2

Also known as

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

Also known asDKFZP564O123 · CHMP2.5 · VPS2B

View full nomenclature history (5)

Alias symbolsDKFZP564O123, CHMP2.5, VPS2B

Previous nameschromatin modifying protein 2B

Alias namesVPS2 homolog B (S. cerevisiae)

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.

Amyotrophic Lateral Sclerosis

Frontotemporal Dementia

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.

Charged multivesicular body proteinsESCRT-III

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.