Entity Details

Primary name STAG3
Entity type gene
Source Source Link

Details

PrimaryID10734
RefseqGeneNG_034114
SymbolSTAG3
Namestromal antigen 3
Chromosome7
Location7q22.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-02-20
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSTAG3_HUMAN

GO terms

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GOName
GO:0000775 chromosome, centromeric region
GO:0000785 chromatin
GO:0000795 synaptonemal complex
GO:0003682 chromatin binding
GO:0005615 extracellular space
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005730 nucleolus
GO:0007062 sister chromatid cohesion
GO:0007130 synaptonemal complex assembly
GO:0008278 cohesin complex
GO:0030893 meiotic cohesin complex

Diseases

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Disease IDSourceNameDescription
615723 OMIMPremature ovarian failure 8 (POF8)An ovarian disorder defined as the cessation of ovarian function under the age of 40 years. It is characterized by oligomenorrhea or amenorrhea, in the presence of elevated levels of serum gonadotropins and low estradiol. The disease is caused by variants affecting the gene represented in this entry. A homozygous deletion in STAG3 predicted to result in frameshift and premature truncation, has been shown to be the cause of premature ovarian failure in a large consanguineous family.