Entity Details

Primary name DJB13_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP59910
EntryNameDJB13_HUMAN
FullNameDnaJ homolog subfamily B member 13
TaxID9606
Evidenceevidence at protein level
Length316
SequenceStatuscomplete
DateCreated2003-10-10
DateModified2021-06-02

Ontological Relatives

GenesDNAJB13

GO terms

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GOName
GO:0005829 cytosol
GO:0005930 axoneme
GO:0031514 motile cilium
GO:0036126 sperm flagellum
GO:0051082 unfolded protein binding
GO:0051085 chaperone cofactor-dependent protein refolding
GO:0051087 chaperone binding
GO:0097224 sperm connecting piece
GO:1904158 axonemal central apparatus assembly

Subcellular Location

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Subcellular Location
Cell projection

Domains

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DomainNameCategoryType
IPR001623 DnaJ domainDomainDomain
IPR002939 Chaperone DnaJ, C-terminalDomainDomain
IPR008971 HSP40/DnaJ peptide-bindingFamilyHomologous superfamily
IPR018253 DnaJ domain, conserved siteSiteConserved site
IPR036869 Chaperone J-domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
617091 OMIMCiliary dyskinesia, primary, 34 (CILD34)A form of primary ciliary dyskinesia, a disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia. CILD34 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry.