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TRAF7

Gene

TNF receptor associated factor 7

HGNCHGNC:20456EnsemblENSG00000131653NCBI Gene84231
Locus: gene with protein productLocation: 16p13.3

Also known as

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

Also known asRFWD1 · RNF119 · DKFZp586I021 · MGC7807
View full nomenclature history (6)
Previous symbolsRFWD1
Alias symbolsRNF119, DKFZp586I021, MGC7807
Previous namesring finger and WD repeat domain 1, TNF receptor-associated factor 7, E3 ubiquitin protein ligase

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.

Meningioma
Genetic Diseases, Inborn
Craniosynostoses

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.

Ring finger proteinsWD repeat domain containingTNF receptor associated factorsZinc fingers TRAF-type

Provenance

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