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FAM227B

Gene

family with sequence similarity 227 member B

HGNCHGNC:26543EnsemblENSG00000166262NCBI Gene196951
Locus: gene with protein productLocation: 15q21.2

Also known as

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

Also known asC15orf33 · FLJ32800
View full nomenclature history (4)
Previous symbolsC15orf33
Alias symbolsFLJ32800
Previous nameschromosome 15 open reading frame 33, family with sequence similarity 227, member B

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.

Basal cell carcinoma
Cartilage Diseases
Hypothyroidism
Actinic keratosis
Graves' Disease
Keloid
Asthma

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.