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MSS51

Gene

MSS51 mitochondrial translational activator

HGNCHGNC:21000EnsemblENSG00000166343NCBI Gene118490
Locus: gene with protein productLocation: 10q22.2

Also known as

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

Also known asZMYND17 · FLJ39565
View full nomenclature history (4)
Previous symbolsZMYND17
Alias symbolsFLJ39565
Previous nameszinc finger, MYND-type containing 17, MSS51 mitochondrial translational activator homolog (S. cerevisiae)

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.

Alcohol drinking
AKT2-related familial partial lipodystrophy

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.

Zinc fingers MYND-type

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.