Entity Details

Primary name CFAP70
Entity type gene
Source Source Link

Details

PrimaryID118491
RefseqGene
SymbolCFAP70
Namecilia and flagella associated protein 70
Chromosome10
Location10q22.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-11-28
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCFA70_HUMAN

GO terms

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GOName
GO:0003341 cilium movement
GO:0005930 axoneme
GO:0036064 ciliary basal body
GO:0036126 sperm flagellum
GO:0036157 outer dynein arm
GO:0060271 cilium assembly
GO:0070062 extracellular exosome

Diseases

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Disease IDSourceNameDescription
618670 OMIMSpermatogenic failure 41 (SPGF41)An autosomal recessive infertility disorder characterized by oligozoospermia, severe asthenozoospermia and flagellar abnormalities such as short, absent, coiled, and irregular-caliber flagella. Some sperm show tapered heads and acrosomal abnormalities. The disease may be caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
CFAP70OBSL1BioGRID31343991 details