MVB12A

Gene

multivesicular body subunit 12A

HGNCHGNC:25153 EnsemblENSG00000141971 NCBI Gene93343

Locus: gene with protein productLocation: 19p13.11

Also known as

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

Also known asFAM125A · FLJ32495

View full nomenclature history (3)

Previous symbolsFAM125A

Alias symbolsFLJ32495

Previous namesfamily with sequence similarity 125, member A

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.

Familial progressive cardiac conduction defect

Wolff-Parkinson's-White syndrome

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.

ESCRT-I

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.