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TRAM2

Gene

translocation associated membrane protein 2

HGNCHGNC:16855EnsemblENSG00000065308NCBI Gene9697
Locus: gene with protein productLocation: 6p12.2

Also known as

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

Also known asKIAA0057
View full nomenclature history (1)
Alias symbolsKIAA0057

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.

Hodgkin's Disease
Male reproductive organ cancer
Gastritis
Osteogenesis Imperfecta
Hypocalcemic vitamin D-resistant rickets
Carcinoma, Hepatocellular
metaphyseal chondrodysplasia, Spahr type

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.

TLC domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.