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RBFA

Gene

ribosome binding factor A

HGNCHGNC:26120EnsemblENSG00000101546NCBI Gene79863
Locus: gene with protein productLocation: 18q23

Also known as

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

Also known asC18orf22 · FLJ21172 · HsT169
View full nomenclature history (5)
Previous symbolsC18orf22
Alias symbolsFLJ21172, HsT169
Previous nameschromosome 18 open reading frame 22, ribosome binding factor A (putative)

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.

Neurodegenerative Diseases
Diabetes, Gestational
Sprain
Lysosomal Storage Diseases
Infections
Major depressive disorder
Metabolic Syndrome
Neoplasms
Autism Spectrum Disorder

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 2025-11-26.
Open TargetsGene–disease associations from the Open Targets Platform.