MPV17

Gene

mitochondrial inner membrane protein MPV17

HGNCHGNC:7224 EnsemblENSG00000115204 NCBI Gene4358

Locus: gene with protein productLocation: 2p23.3

Also known as

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

Also known asSYM1

View full nomenclature history (3)

Alias symbolsSYM1

Previous namesMpV17 transgene, murine homolog, glomerulosclerosis

Alias namesglomerulosclerosis

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.

Cholestasis

Liver Failure

Mitochondrial Diseases

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.

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.