Entity Details

Primary name CFAP251
Entity type gene
Source Source Link

Details

PrimaryID144406
RefseqGeneNG_021364
SymbolCFAP251
Namecilia and flagella associated protein 251
Chromosome12
Location12q24.31
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-01-21
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCF251_HUMAN

GO terms

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GOName
GO:0003341 cilium movement
GO:0005930 axoneme
GO:0030317 flagellated sperm motility
GO:0031514 motile cilium
GO:0036126 sperm flagellum

Diseases

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Disease IDSourceNameDescription
618152 OMIMSpermatogenic failure 33 (SPGF33)An autosomal recessive infertility disorder caused by spermatogenesis defects that result in multiple abnormalities of sperm flagellum, including short, bent, curled, thick, or absent flagella. The disease is caused by variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
CFAP251HSPB1BioGRID, IntAct25277244 details
CFAP251CLK1BioGRID26167880 details
CFAP251ESR2BioGRID29509190 details
CFAP251DDX58BioGRID32513696 details