Entity Details

Primary name TTC29_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8NA56
EntryNameTTC29_HUMAN
FullNameTetratricopeptide repeat protein 29
TaxID9606
Evidenceevidence at protein level
Length475
SequenceStatuscomplete
DateCreated2007-07-10
DateModified2021-06-02

Ontological Relatives

GenesTTC29

GO terms

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GOName
GO:0003341 cilium movement
GO:0005737 cytoplasm
GO:0005856 cytoskeleton
GO:0036126 sperm flagellum
GO:0044782 cilium organization

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR011990 Tetratricopeptide-like helical domain superfamilyFamilyHomologous superfamily
IPR019734 Tetratricopeptide repeatRepeatRepeat

Diseases

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Disease IDSourceNameDescription
618745 OMIMSpermatogenic failure 42 (SPGF42)An autosomal recessive infertility disorder characterized by almost immotile spermatozoa due to multiple morphologic abnormalities of the flagella, including short, absent, coiled, and bent flagella. Some spermatozoa also show abnormalities of the head, acrosome, midpiece, or endpiece. The disease is caused by variants affecting the gene represented in this entry.

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
TTC29_HUMANZMY12_HUMANBioGRID32296183 details
TTC29_HUMANABCE1_HUMANBioGRID25659154 details