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ZGRF1

Gene

zinc finger GRF-type containing 1

HGNCHGNC:25654EnsemblENSG00000138658NCBI Gene55345
Locus: gene with protein productLocation: 4q25

Also known as

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

Also known asC4orf21 · FLJ11331
View full nomenclature history (3)
Previous symbolsC4orf21
Alias symbolsFLJ11331
Previous nameschromosome 4 open reading frame 21

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.

Autism Spectrum Disorder
Atrial Fibrillation
Cerebrovascular Disorders

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 GRF-typeUPF1 like RNA helicases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-07-04.
Open TargetsGene–disease associations from the Open Targets Platform.