Hs02350244_cn

• Gene Symbol: ST7L
• Assay Reference Genome Location: Chr.1:112541927 on build GRCh38
• Cytoband: 1p13.2

Target Gene Details

• Entrez Gene ID: 54879
• Gene Name: suppression of tumorigenicity 7 like
• Gene Aliases: FAM4B, ST7R, STLR
• Location: Chr.1:112517444-112620838 on Build GRCh38
• Assay Gene Location: Within Exon 19

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ST7L	NM_001308264.1			NP_001295193.1
	NM_017744.4			NP_060214.2
	NM_138727.3			NP_620055.1
	NM_138728.2			NP_620056.1
	NM_138729.3	14	1958	NP_620057.1
	XM_005270963.4			XP_005271020.1
	XM_005270964.3			XP_005271021.1
	XM_011541627.2			XP_011539929.1
	XM_011541628.2			XP_011539930.1
	XM_011541629.2			XP_011539931.1
	XM_011541630.2			XP_011539932.1
	XM_011541631.2			XP_011539933.1
	XM_017001534.1			XP_016857023.1
	XM_017001536.1			XP_016857025.1
	XM_017001537.1			XP_016857026.1
	XM_017001538.1			XP_016857027.1
	AB081317.1			BAB88871.1
	AB081318.1			BAB88872.1
	AB081319.1			BAB88873.1
	AB081320.1	14	1729	BAB88874.1
	AK000291.1			BAA91060.1
	AK021719.1
	AK095837.1
	AK097837.1			BAC05180.1
	AK225307.1
	AK291042.1
	AK295507.1
	AK295955.1
	AK301869.1	14	1659
	BC037830.1	15	2448	AAH37830.1
	BC065501.1			AAH65501.1
	BX537988.1			CAD97948.1
	BX538338.1			CAD98103.1
	BX640667.1	14	1634	CAE45803.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv831081	Chr.1:112392298 - 112580018 on Build GRCh38	Loss	ST7L MIR4256 CTTNBP2NL WNT2B
esv27061	Chr.1:112150007 - 112703641 on Build GRCh38	Gain+Loss	ST7L MIR4256 CTTNBP2NL WNT2B CAPZA1 MOV10 RHOC

More Information

• Set Membership: Intragenic, Exonic, DGV Variation

Gene Ontology Categories:

Process(es)

negative regulation of cell growth