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MCM3AP

Gene

minichromosome maintenance complex component 3 associated protein

HGNCHGNC:6946EnsemblENSG00000160294NCBI Gene8888
Locus: gene with protein productLocation: 21q22.3

Also known as

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

Also known asMap80 · KIAA0572 · GANP · SAC3
View full nomenclature history (7)
Alias symbolsMap80, KIAA0572, GANP, SAC3
Previous namesMCM3 minichromosome maintenance deficient 3 (S. cerevisiae) associated protein, minichromosome maintenance deficient (S. cerevisiae) 3-associated protein
Alias namesgerminal-centre associated nuclear protein

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.

Genetic Diseases, Inborn
Autism Spectrum Disorder
Neurodegenerative Diseases
Mental Disorders
Testicular Neoplasms
Premature Birth
Congenital fibrosis of the extraocular muscles

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.

Lysine acetyltransferasesTranscription and export complex 2

Provenance

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