SOX2

Description: This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). [provided by RefSeq, Jul 2008]
Full Name: SRY-box transcription factor 2; Source NCBI

All peaks SOX2

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Non redundant peaks SOX2

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SEQUENCES SOX2

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Target name	Target modification	Ecotype/Strain	Biotype	Biotype modification	Source	Species	Experiment	Peaks
SOX2			BJ	INDUCED	GEO	Homo sapiens	GSE36570	121,462
SOX2			glioma	stem	GEO	Homo sapiens	GSE67282	3,859
SOX2			hESC		GEO	Homo sapiens	GSE18292	18,963
SOX2			hESC		GEO	Homo sapiens	GSE69479	2,352
SOX2			HNSC		GEO	Homo sapiens	GSE69479	74,636
SOX2			KYSE70		GEO	Homo sapiens	GSE46837	6,840
SOX2			RENVM		GEO	Homo sapiens	GSE49404	38,149
SOX2			RENVM	SHSOX2	GEO	Homo sapiens	GSE49404	4,497
SOX2			TT		GEO	Homo sapiens	GSE46837	10,181
SOX2			H9		GEO	Homo sapiens	GSE46837	3,216
SOX2			hiPSC		GEO	Homo sapiens	GSE56567	64,223
SOX2			hiPSC		GEO	Homo sapiens	GSE67282	6,645
SOX2			hiPSC	INHI	GEO	Homo sapiens	GSE67282	3,238
SOX2			hiPSC	KDP53	GEO	Homo sapiens	GSE67282	5,025
SOX2			hiPSC	KDP53_INHI	GEO	Homo sapiens	GSE67282	6,198
SOX2			hiPSC	3s2	GEO	Homo sapiens	GSE81899	879
SOX2			OSK		GEO	Homo sapiens	GSE81899	1,237
SOX2			OSKM		GEO	Homo sapiens	GSE81899	5,507
SOX2			OSvK		GEO	Homo sapiens	GSE81899	263
SOX2			OSvKM		GEO	Homo sapiens	GSE81899	257
Target name	Target modification	Ecotype/Strain	Biotype	Biotype modification	Source	Species	Experiment	Peaks