STAG3
Cohesin subunit SA-3
Also known as: STAG3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UJ98
- Gene
- STAG3
- Ensembl
- ENSG00000066923
- Chromosome
- 7
- Canonical length
- 1225 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli
OverviewNCBI Gene
The protein encoded by this gene is expressed in the nucleus and is a subunit of the cohesin complex which regulates the cohesion of sister chromatids during cell division. A mutation in this gene is associated with premature ovarian failure. Alternate splicing results in multiple transcript variants encoding distinct isoforms. This gene has multiple pseudogenes. [provided by RefSeq, Apr 2014]
Canonical amino-acid sequenceUniProt
1225 residues, UniProt reviewed canonical sequence.
>Q9UJ98|STAG3
1 MSSPLQRAVG DTKRALSASS SSSASLPFDD RDSNHTSEGN GDSLLADEDT DFEDSLNRNV
61 KKRAAKRPPK TTPVAKHPKK GSRVVHRHSR KQSEPPANDL FNAVKAAKSD MQSLVDEWLD
121 SYKQDQDAGF LELVNFFIQS CGCKGIVTPE MFKKMSNSEI IQHLTEQFNE DSGDYPLIAP
181 GPSWKKFQGS FCEFVRTLVC QCQYSLLYDG FPMDDLISLL TGLSDSQVRA FRHTSTLAAM
241 KLMTSLVKVA LQLSVHQDNN QRQYEAERNK GPGQRAPERL ESLLEKRKEL QEHQEEIEGM
301 MNALFRGVFV HRYRDVLPEI RAICIEEIGC WMQSYSTSFL TDSYLKYIGW TLHDKHREVR
361 LKCVKALKGL YGNRDLTTRL ELFTSRFKDR MVSMVMDREY DVAVEAVRLL ILILKNMEGV
421 LTDADCESVY PVVYASHRGL ASAAGEFLYW KLFYPECEIR MMGGREQRQS PGAQRTFFQL
481 LLSFFVESEL HDHAAYLVDS LWDCAGARLK DWEGLTSLLL EKDQNLGDVQ ESTLIEILVS
541 SARQASEGHP PVGRVTGRKG LTSKERKTQA DDRVKLTEHL IPLLPQLLAK FSADAEKVTP
601 LLQLLSCFDL HIYCTGRLEK HLELFLQQLQ EVVVKHAEPA VLEAGAHALY LLCNPEFTFF
661 SRADFARSQL VDLLTDRFQQ ELEELLQSSF LDEDEVYNLA ATLKRLSAFY NTHDLTRWEL
721 YEPCCQLLQK AVDTGEVPHQ VILPALTLVY FSILWTLTHI SKSDASQKQL SSLRDRMVAF
781 CELCQSCLSD VDTEIQEQAF VLLSDLLLIF SPQMIVGGRD FLRPLVFFPE ATLQSELASF
841 LMDHVFIQPG DLGSGDSQED HLQIERLHQR RRLLAGFCKL LLYGVLEMDA ASDVFKHYNK
901 FYNDYGDIIK ETLTRARQID RSHCSRILLL SLKQLYTELL QEHGPQGLNE LPAFIEMRDL
961 ARRFALSFGP QQLQNRDLVV MLHKEGIQFS LSELPPAGSS NQPPNLAFLE LLSEFSPRLF
1021 HQDKQLLLSY LEKCLQHVSQ APGHPWGPVT TYCHSLSPVE NTAETSPQVL PSSKRRRVEG
1081 PAKPNREDVS SSQEESLQLN SIPPTPTLTS TAVKSRQPLW GLKEMEEEDG SELDFAQGQP
1141 VAGTERSRFL GPQYFQTPHN PSGPGLGNQL MRLSLMEEDE EEELEIQDES NEERQDTDMQ
1201 ASSYSSTSER GLDLLDSTEL DIEDFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against STAG3 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 50 nTPM
Expression across tissuesHPA
Tissue
- testis: 50 nTPM
- bone marrow: 1 nTPM
- heart muscle: 0.8 nTPM
- thymus: 0.5 nTPM
- esophagus: 0.4 nTPM
- kidney: 0.4 nTPM
Single-cell type
- oocytes: 1,340 nCPM
- early primary spermatocytes: 230 nCPM
- b-cells: 128 nCPM
- myonuclei: 106 nCPM
- epicardial cells: 84 nCPM
- retinal horizontal cells: 72 nCPM
Immune cell
- non-classical monocyte: 1.3 nTPM
- plasmacytoid DC: 0.9 nTPM
- intermediate monocyte: 0.8 nTPM
- classical monocyte: 0.7 nTPM
- eosinophil: 0.7 nTPM
- memory CD8 T-cell: 0.7 nTPM
Brain region
- thalamus: 1.5 nTPM
- cerebellum: 1.3 nTPM
- cerebral cortex: 1.3 nTPM
- white matter: 1.3 nTPM
- medulla oblongata: 1.2 nTPM
- basal ganglia: 1.1 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about STAG3.
Disease | AllUniProt
Conditions STAG3 is implicated in, by any mechanism.
- Premature ovarian failure 8 (POF8) MIM:615723
- Spermatogenic failure 61 (SPGF61) MIM:619672
Disease | GeneticClinVar
27 pathogenic / likely-pathogenic of 278 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Premature ovarian failure 8
- Spermatogenic failure 61
- Premature ovarian insufficiency
- Non-obstructive azoospermia
- Spermatogenesis maturation arrest
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.61
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.66
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- establishment of meiotic sister chromatid cohesion
- sister chromatid cohesion
- synaptonemal complex assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of STAG3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads STAG3 as an antibody target. Whether an autoantibody or antibody against STAG3 could matter depends on whether native STAG3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
STAG3 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label STAG3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...