ATP5MK

Gene

ATP synthase membrane subunit k

HGNCHGNC:30889 EnsemblENSG00000173915 NCBI Gene84833

Locus: gene with protein productLocation: 10q24.33

Also known as

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

Also known asUSMG5 · ATP5MD · MGC14697 · bA792D24.4 · DAPIT · AGP

View full nomenclature history (11)

Previous symbolsUSMG5, ATP5MD

Alias symbolsMGC14697, bA792D24.4, DAPIT, AGP

Previous namesupregulated during skeletal muscle growth 5, upregulated during skeletal muscle growth 5 homolog (mouse), up-regulated during skeletal muscle growth 5 homolog (mouse), ATP synthase membrane subunit DAPIT

Alias namesDiabetes Associated Protein in Insulin-sensitive Tissues

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.

Sleep Initiation and Maintenance Disorders

Mitochondrial Diseases

Renal Insufficiency

Malaria

Depressive Disorder

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.

Mitochondrial complex V: ATP synthase subunitsMicroRNA protein coding host genes

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.