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TUT7

Gene

terminal uridylyl transferase 7

HGNCHGNC:25817EnsemblENSG00000083223NCBI Gene79670
Locus: gene with protein productLocation: 9q21.33

Also known as

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

Also known asZCCHC6 · KIAA1711 · FLJ13409 · PAPD6 · TENT3B
View full nomenclature history (7)
Previous symbolsZCCHC6
Alias symbolsKIAA1711, FLJ13409, PAPD6, TENT3B
Previous nameszinc finger CCHC-type containing 6
Alias namesTUTase7

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.

Atrial Fibrillation
Ocular Hypertension
Placental abruption
Sjogren's Syndrome
Neoplasms
Pericarditis
Joint Diseases
Placental retention

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.

Zinc fingers CCHC-typeNon-canonical poly(A) polymerasesTerminal nucleotidyltransferases

Provenance

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