Entity Details

Primary name TXN4A_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP83876
EntryNameTXN4A_HUMAN
FullNameThioredoxin-like protein 4A
TaxID9606
Evidenceevidence at protein level
Length142
SequenceStatuscomplete
DateCreated2004-04-26
DateModified2021-06-02

Ontological Relatives

GenesTXNL4A

GO terms

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GOName
GO:0000245 spliceosomal complex assembly
GO:0000375 RNA splicing, via transesterification reactions
GO:0000398 mRNA splicing, via spliceosome
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005681 spliceosomal complex
GO:0005682 U5 snRNP
GO:0005829 cytosol
GO:0007049 cell cycle
GO:0031965 nuclear membrane
GO:0046540 U4/U6 x U5 tri-snRNP complex
GO:0051301 cell division
GO:0071005 U2-type precatalytic spliceosome

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR004123 Dim1 familyFamilyFamily
IPR036249 Thioredoxin-like superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
608572 OMIMBurn-McKeown syndrome (BMKS)A disease characterized by choanal atresia, sensorineural deafness, cardiac defects, and typical craniofacial dysmorphism consisting of narrow palpebral fissures, coloboma of the lower eyelids, prominent nose with high nasal bridge, short philtrum, cleft lip and/or palate, and large and protruding ears. Intellectual development is normal. The disease is caused by variants affecting the gene represented in this entry.