FRRS1L

Gene

ferric chelate reductase 1 like

HGNCHGNC:1362 EnsemblENSG00000260230 NCBI Gene23732

Locus: gene with protein productLocation: 9q31.3

Also known as

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

Also known asC9orf4 · CG-6

View full nomenclature history (4)

Previous symbolsC9orf4

Alias symbolsCG-6

Previous nameschromosome 9 open reading frame 4, ferric-chelate reductase 1-like

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.

Genetic developmental and epileptic encephalopathy

Genetic Diseases, Inborn

Autosomal recessive non-syndromic intellectual disability

Obesity disorder

Ovarian dysfunction

Diabetes Mellitus, Type 2

Epilepsy

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.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.