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TMEM38B

Gene

transmembrane protein 38B

HGNCHGNC:25535EnsemblENSG00000095209NCBI Gene55151
Locus: gene with protein productLocation: 9q31.2

Also known as

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

Also known asC9orf87 · FLJ10493 · bA219P18.1 · D4Ertd89e · TRIC-B
View full nomenclature history (6)
Previous symbolsC9orf87
Alias symbolsFLJ10493, bA219P18.1, D4Ertd89e, TRIC-B
Previous nameschromosome 9 open reading frame 87

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.

Osteogenesis Imperfecta
Drug Hypersensitivity
Placental abruption
Urolithiasis

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 2023-03-27.
Open TargetsGene–disease associations from the Open Targets Platform.