SSX1

SSX1
Identifiers
Aliases	SSX1, CT5.1, SSRC, synovial sarcoma, X breakpoint 1, SSX family member 1
External IDs	OMIM: 312820; HomoloGene: 136735; GeneCards: SSX1; OMA:SSX1 - orthologs
Gene location (Human)
Chr.	X chromosome (human)
End	48,267,444 bp
RNA expression pattern
	Top expressed in
	uterine tube; ; human musculoskeletal system; ; muscular system; ; muscle; ; muscle; ; thyroid gland; ; left lobe of thyroid gland; ; blood; ; right lobe of thyroid gland; ; lower leg;
	n/a
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	protein binding; transcription corepressor activity; nucleic acid binding;
Cellular component	intracellular anatomical structure; nucleus;
Biological process	regulation of transcription, DNA-templated; transcription, DNA-templated; negative regulation of nucleic acid-templated transcription;
	Sources:Amigo / QuickGO
Orthologs
	6756
	n/a
	ENSG00000126752
	n/a
	Q16384
	n/a
	NM_005635; NM_001278691
	n/a
	NP_001265620; NP_005626
	n/a
	Wikidata
View/Edit Human

Protein SSX1 is a protein that in humans is encoded by the SSX1 gene.^[3]^[4]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000126752 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ de Leeuw B, Balemans M, Olde Weghuis D, Geurts van Kessel A (Oct 1995). "Identification of two alternative fusion genes, SYT-SSX1 and SYT-SSX2, in t(X;18)(p11.2;q11.2)-positive synovial sarcomas". Hum Mol Genet. 4 (6): 1097–9. doi:10.1093/hmg/4.6.1097. PMID 7655467.
^ "Entrez Gene: SSX1 synovial sarcoma, X breakpoint 1".