Entity Details

Primary name TXND3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8N427
EntryNameTXND3_HUMAN
FullNameThioredoxin domain-containing protein 3
TaxID9606
Evidenceevidence at transcript level
Length588
SequenceStatuscomplete
DateCreated2005-07-05
DateModified2021-06-02

Ontological Relatives

GenesNME8

GO terms

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GOName
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005930 axoneme
GO:0007275 multicellular organism development
GO:0007283 spermatogenesis
GO:0008017 microtubule binding
GO:0016607 nuclear speck
GO:0030154 cell differentiation
GO:0030317 flagellated sperm motility
GO:0034614 cellular response to reactive oxygen species
GO:0036157 outer dynein arm
GO:0060271 cilium assembly
GO:0097225 sperm midpiece
GO:0097228 sperm principal piece
GO:0097598 sperm cytoplasmic droplet

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR013766 Thioredoxin domainDomainDomain
IPR017937 Thioredoxin, conserved siteSiteConserved site
IPR034907 Nucleoside diphosphate kinase-like domainDomainDomain
IPR036249 Thioredoxin-like superfamilyFamilyHomologous superfamily
IPR036850 Nucleoside diphosphate kinase-like domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
610852 OMIMCiliary dyskinesia, primary, 6 (CILD6)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; reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the patients exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome. The disease is caused by variants affecting the gene represented in this entry.