Entity Details

Primary name BDP1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionA6H8Y1
EntryNameBDP1_HUMAN
FullNameTranscription factor TFIIIB component B'' homolog
TaxID9606
Evidenceevidence at protein level
Length2624
SequenceStatuscomplete
DateCreated2008-05-20
DateModified2021-06-02

Ontological Relatives

GenesBDP1

GO terms

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GOName
GO:0000126 transcription factor TFIIIB complex
GO:0001156 TFIIIC-class transcription factor complex binding
GO:0005654 nucleoplasm
GO:0070898 RNA polymerase III preinitiation complex assembly

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR001005 SANT/Myb domainDomainDomain
IPR009057 Homeobox-like domain superfamilyFamilyHomologous superfamily
IPR039467 Transcription factor TFIIIB component B'', Myb domainDomainDomain

Diseases

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Disease IDSourceNameDescription
618257 OMIMDeafness, autosomal recessive, 112 (DFNB112)A form of non-syndromic, sensorineural deafness characterized by postlingual progressive hearing impairment. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. The disease may be caused by variants affecting the gene represented in this entry.

Interactions

4 interactions