CFAP47

Gene

cilia and flagella associated protein 47

HGNCHGNC:26708 EnsemblENSG00000165164 NCBI Gene286464

Locus: gene with protein productLocation: Xp21.1

Also known as

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

Also known asCXorf59 · CXorf22 · CXorf30 · CHDC2 · FLJ36601 · RP13-11B7.1 · MGC34831

View full nomenclature history (11)

Previous symbolsCXorf59, CXorf22, CXorf30, CHDC2

Alias symbolsFLJ36601, RP13-11B7.1, MGC34831

Previous nameschromosome X open reading frame 59, chromosome X open reading frame 22, chromosome X open reading frame 30, calponin homology domain containing 2

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.

Polycystic Kidney Diseases

Genetic Diseases, Inborn

Retinitis Pigmentosa

Spermatogenic failure

Non-syndromic male infertility due to sperm motility 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.

Gene family

HGNC gene-group membership.

Cilia and flagella associated

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-08-02.

Open TargetsGene–disease associations from the Open Targets Platform.