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IMMP2L

Gene

inner mitochondrial membrane peptidase subunit 2

HGNCHGNC:14598EnsemblENSG00000184903NCBI Gene83943
Locus: gene with protein productLocation: 7q31.1

Also known as

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

Also known asIMMP2L-IT1 · IMP2
View full nomenclature history (5)
Previous symbolsIMMP2L-IT1
Alias symbolsIMP2
Previous namesIMP2 inner mitochondrial membrane protease-like (S. cerevisiae), IMMP2L intronic transcript 1 (non-protein coding), IMP2 inner mitochondrial membrane peptidase-like (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.

Schizophrenia
Smoking initiation
Attention Deficit Disorder with Hyperactivity
Obsessive-Compulsive Disorder
Sleep Initiation and Maintenance Disorders
Pericarditis
Obesity disorder
Osteoarthritis, Knee
Spinal Cord Injuries

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.