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MVB12B

Gene

multivesicular body subunit 12B

HGNCHGNC:23368EnsemblENSG00000196814NCBI Gene89853
Locus: gene with protein productLocation: 9q33.3

Also known as

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

Also known asC9orf28 · FAM125B · FLJ00001
View full nomenclature history (5)
Previous symbolsC9orf28, FAM125B
Alias symbolsFLJ00001
Previous nameschromosome 9 open reading frame 28, family with sequence similarity 125, 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.

HIV Infections
Virus Diseases
Alopecia
Placental retention
Spinal Cord Injuries
Diabetes Mellitus
Bipolar Disorder
Risk-taking behaviour

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.