Back to discover

MPV17L

Gene

MPV17 mitochondrial inner membrane protein like

HGNCHGNC:26827EnsemblENSG00000156968NCBI Gene255027
Locus: gene with protein productLocation: 16p13.11

Also known as

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

Also known asFLJ39599 · M-LPH · M-LPH1 · M-LPH2 · MPV17L1
View full nomenclature history (6)
Alias symbolsFLJ39599, M-LPH, M-LPH1, M-LPH2, MPV17L1
Alias namesHuman Mpv17-like 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.

autosomal dominant hyperinsulinism due to Kir6.2 deficiency
diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
Hyperinsulinemic hypoglycemia, familial, 2
GCGR-related hyperglucagonemia
Smoking initiation
autosomal dominant hyperinsulinism due to SUR1 deficiency
Hyperinsulinemic hypoglycemia, familial, 1

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 2023-08-07.
Open TargetsGene–disease associations from the Open Targets Platform.