Entity Details

Primary name BRDT_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ58F21
EntryNameBRDT_HUMAN
FullNameBromodomain testis-specific protein
TaxID9606
Evidenceevidence at protein level
Length947
SequenceStatuscomplete
DateCreated2006-05-30
DateModified2021-06-02

Ontological Relatives

GenesBRDT

GO terms

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GOName
GO:0001207 histone displacement
GO:0003713 transcription coactivator activity
GO:0005634 nucleus
GO:0006338 chromatin remodeling
GO:0006355 regulation of transcription, DNA-templated
GO:0006397 mRNA processing
GO:0007140 male meiotic nuclear division
GO:0007141 male meiosis I
GO:0007283 spermatogenesis
GO:0008380 RNA splicing
GO:0030154 cell differentiation
GO:0042393 histone binding
GO:0043484 regulation of RNA splicing
GO:0051039 positive regulation of transcription involved in meiotic cell cycle
GO:0070577 lysine-acetylated histone binding

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR001487 BromodomainDomainDomain
IPR018359 Bromodomain, conserved siteSiteConserved site
IPR027353 NET domainDomainDomain
IPR031354 Bromodomain protein 4, C-terminalDomainDomain
IPR036427 Bromodomain-like superfamilyFamilyHomologous superfamily
IPR038336 NET domain superfamilyFamilyHomologous superfamily
IPR043508 Brdt, bromodomain, repeat IDomainDomain
IPR043509 Brdt, bromodomain, repeat IIDomainDomain

Diseases

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Disease IDSourceNameDescription
617644 OMIMSpermatogenic failure 21 (SPGF21)An infertility disorder caused by spermatogenesis defects and characterized by acephalic spermatozoa in the semen of affected individuals. SPGF21 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry.

Interactions

5 interactions