Hs00985032_cn

• Gene Symbol: ST7L
• Assay Reference Genome Location: Chr.1:112525087 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 22

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ST7L	NM_001308264.1	14	2750	NP_001295193.1
	NM_017744.4	15	2959	NP_060214.2
	NM_138727.3	15	2908	NP_620055.1
	NM_138728.2	14	2866	NP_620056.1
	XM_005270963.4	15	2482	XP_005271020.1
	XM_005270964.3	14	2574	XP_005271021.1
	XM_011541628.2			XP_011539930.1
	XM_011541629.2	15	2682	XP_011539931.1
	XM_011541630.2	15	3378	XP_011539932.1
	XM_011541631.2	15	2506	XP_011539933.1
	XM_017001536.1	13	2481	XP_016857025.1
	XM_017001537.1	12	2301	XP_016857026.1
	XM_017001538.1	13	2294	XP_016857027.1
	AK000291.1	4	1405	BAA91060.1
	AK095837.1	12	2174
	AK225307.1	4	1405
	BX537988.1	17	2915	CAD97948.1
	BX538338.1	9	1890	CAD98103.1

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	CTTNBP2NL ST7L WNT2B MIR4256
esv27061	Chr.1:112150007 - 112703641 on Build GRCh38	Gain+Loss	CTTNBP2NL MOV10 ST7L RHOC WNT2B MIR4256 CAPZA1

More Information

Additional Information:

For this assay, SNP(s) [rs114323109] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Exonic, DGV Variation

Gene Ontology Categories:

Process(es)

negative regulation of cell growth