Entity Details

Primary name TDRD9_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8NDG6
EntryNameTDRD9_HUMAN
FullNameATP-dependent RNA helicase TDRD9
TaxID9606
Evidenceevidence at transcript level
Length1382
SequenceStatuscomplete
DateCreated2008-05-20
DateModified2021-06-02

Ontological Relatives

GenesTDRD9

GO terms

Show/Hide Table
GOName
GO:0003723 RNA binding
GO:0003724 RNA helicase activity
GO:0005524 ATP binding
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0007140 male meiotic nuclear division
GO:0007141 male meiosis I
GO:0007275 multicellular organism development
GO:0007283 spermatogenesis
GO:0009566 fertilization
GO:0010529 negative regulation of transposition
GO:0016887 ATP hydrolysis activity
GO:0030154 cell differentiation
GO:0031047 gene silencing by RNA
GO:0034587 piRNA metabolic process
GO:0043046 DNA methylation involved in gamete generation
GO:0071547 piP-body

Subcellular Location

Show/Hide Table
Subcellular Location
Cytoplasm
Nucleus

Domains

Show/Hide Table
DomainNameCategoryType
IPR001650 Helicase, C-terminalDomainDomain
IPR002999 Tudor domainDomainDomain
IPR007502 Helicase-associated domainDomainDomain
IPR011545 DEAD/DEAH box helicase domainDomainDomain
IPR014001 Helicase superfamily 1/2, ATP-binding domainDomainDomain
IPR027417 P-loop containing nucleoside triphosphate hydrolaseFamilyHomologous superfamily
IPR035437 SNase-like, OB-fold superfamilyFamilyHomologous superfamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
618110 OMIMSpermatogenic failure 30 (SPGF30)An autosomal recessive infertility disorder caused by spermatogenesis defects that result in non-obstructive azoospermia or cryptozoospermia. The disease is caused by variants affecting the gene represented in this entry.

Interactions

0 interactions

InteractorPartnerSourcesPublicationsLink