Entity Details

Primary name TDRD9
Entity type gene
Source Source Link

Details

PrimaryID122402
RefseqGene
SymbolTDRD9
Nametudor domain containing 9
Chromosome14
Location14q32.33
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-11-29
ModificationDate2021-06-22

Ontological Relatives

UniProt IDsTDRD9_HUMAN

GO terms

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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

Diseases

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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

4 interactions

InteractorPartnerSourcesPublicationsLink
TDRD9DNAJC7BioGRID, IntAct26496610 details
TDRD9PPP2R1ABioGRID23443559 details
TDRD9TRIM25BioGRID29117863 details
TDRD9VIRMABioGRID29507755 details