Entity Details

Primary name TEX15_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9BXT5
EntryNameTEX15_HUMAN
FullNameTestis-expressed protein 15
TaxID9606
Evidenceevidence at transcript level
Length2789
SequenceStatuscomplete
DateCreated2006-06-27
DateModified2021-06-02

Ontological Relatives

GO terms

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GOName
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0006281 DNA repair
GO:0006306 DNA methylation
GO:0007129 homologous chromosome pairing at meiosis
GO:0007140 male meiotic nuclear division
GO:0007283 spermatogenesis
GO:0010529 negative regulation of transposition
GO:0010569 regulation of double-strand break repair via homologous recombination
GO:0030154 cell differentiation
GO:0031047 gene silencing by RNA

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus

Domains

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DomainNameCategoryType
IPR026616 Testis-expressed sequence 15 proteinFamilyFamily
IPR032765 Testis expressed sequence 15 domainDomainDomain

Diseases

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Disease IDSourceNameDescription
617960 OMIMSpermatogenic failure 25 (SPGF25)An autosomal recessive infertility disorder caused by spermatogenesis defects that result in severe oligozoospermia or azoospermia. The disease is caused by variants affecting the gene represented in this entry.

Interactions

3 interactions