Entity Details

Primary name CFA65_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ6ZU64
EntryNameCFA65_HUMAN
FullNameCilia- and flagella-associated protein 65
TaxID9606
Evidenceevidence at protein level
Length1925
SequenceStatuscomplete
DateCreated2007-05-29
DateModified2021-06-02

Ontological Relatives

GenesCFAP65

GO terms

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GOName
GO:0001669 acrosomal vesicle
GO:0002080 acrosomal membrane
GO:0003723 RNA binding
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0007288 sperm axoneme assembly
GO:0016021 integral component of membrane
GO:0030317 flagellated sperm motility
GO:0036126 sperm flagellum
GO:0097225 sperm midpiece

Subcellular Location

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Subcellular Location
Cell projection
Cytoplasm
Cytoplasmic vesicle

Domains

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DomainNameCategoryType
IPR000535 Major sperm protein (MSP) domainDomainDomain
IPR013783 Immunoglobulin-like foldFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
618664 OMIMSpermatogenic failure 40 (SPGF40)An autosomal recessive infertility disorder characterized by severely reduced or absent sperm motility, due to multiple morphologic anomalies such as absent, short, bent, coiled and irregular-caliber tails. Patient spermatozoa may also show morphologic defects of the sperm head. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
CFA65_HUMANCCDB1_HUMANBioGRID, IntAct25416956 details