MCM9

Gene

minichromosome maintenance 9 homologous recombination repair factor

HGNCHGNC:21484 EnsemblENSG00000111877 NCBI Gene254394

Locus: gene with protein productLocation: 6q22.31

Also known as

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

Also known asMCMDC1 · C6orf61 · MGC35304 · dJ329L24.3 · FLJ20170

View full nomenclature history (8)

Previous symbolsMCMDC1, C6orf61

Alias symbolsMGC35304, dJ329L24.3, FLJ20170

Previous namesminichromosome maintenance deficient domain containing 1, chromosome 6 open reading frame 61, minichromosome maintenance complex component 9

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.

46,XX gonadal dysgenesis

Neurodegenerative Diseases

Primary Ovarian Insufficiency

Male reproductive organ cancer

Placental abruption

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.

MCM 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.