TMEM95

Gene

transmembrane protein 95

HGNCHGNC:27898 EnsemblENSG00000182896 NCBI Gene339168

Locus: gene with protein productLocation: 17p13.1

Also known as

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

Also known asMGC129793 · UNQ9390

View full nomenclature history (2)

Alias symbolsMGC129793, UNQ9390

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.

Metabolic Syndrome

Arrhythmias, Cardiac

Cardiac Conduction System Disease

Familial progressive cardiac conduction defect

Conduct Disorder

Infertility, Male

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.

Gamete adhesion and fusion factors

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-03-12.

Open TargetsGene–disease associations from the Open Targets Platform.