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TMEM135

Gene

transmembrane protein 135

HGNCHGNC:26167EnsemblENSG00000166575NCBI Gene65084
Locus: gene with protein productLocation: 11q14.2

Also known as

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

Also known asFLJ22104 · PMP52
View full nomenclature history (3)
Alias symbolsFLJ22104, PMP52
Alias namesperoxisomal protein 52

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.

Osteoporosis
Fractures, Bone
Glaucoma
Polycystic Ovary Syndrome
Ovarian neoplasm
Tibial Fractures

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.

Tim17 family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-10-23.
Open TargetsGene–disease associations from the Open Targets Platform.