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RELT

Gene

RELT TNF receptor

HGNCHGNC:13764EnsemblENSG00000054967NCBI Gene84957
Locus: gene with protein productLocation: 11q13.4

Also known as

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

Also known asTNFRSF19L · FLJ14993
View full nomenclature history (5)
Previous symbolsTNFRSF19L
Alias symbolsFLJ14993
Previous namestumor necrosis factor receptor superfamily, member 19-like, RELT tumor necrosis factor receptor
Alias namesreceptor expressed in lymphoid tissues

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.

Amelogenesis imperfecta
Crohn's Disease

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.

Tumor necrosis factor receptor superfamilyRELT family

Provenance

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