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RNF207

Gene

ring finger protein 207

HGNCHGNC:32947EnsemblENSG00000158286NCBI Gene388591
Locus: gene with protein productLocation: 1p36.31

Also known as

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

Also known asC1orf188 · FLJ46380 · FLJ32096
View full nomenclature history (5)
Previous symbolsC1orf188
Alias symbolsFLJ46380, FLJ32096
Previous nameschromosome 1 open reading frame 188
Alias namesOTTHUMG00000001089

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
Cardiomyopathy, Hypertrophic
Atrioventricular Block
Neurodegenerative Diseases
Heart Failure
Arrhythmias, Cardiac
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.

Ring finger proteins

Provenance

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