Hs02667513_cn

• Gene Symbol: XKR9
• Assay Reference Genome Location: Chr.8:70707002 on build GRCh38
• Cytoband: 8q13.3

Target Gene Details

• Entrez Gene ID: 389668
• Gene Name: XK related 9
• Gene Aliases: XRG9
• Location: Chr.8:70669365-71066635 on Build GRCh38
• Assay Gene Location: Within Exon 8

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
XKR9	NM_001011720.1	4	876	NP_001011720.1
	NM_001287258.1	5	994	NP_001274187.1
	NM_001287259.1	5	986	NP_001274188.1
	NM_001287260.1	4	730	NP_001274189.1
	XM_006716447.3	2	226	XP_006716510.1
	XM_011517524.2	4	859	XP_011515826.1
	XM_011517525.2	4	721	XP_011515827.1
	XM_011517526.2	4	871	XP_011515828.1
	XM_011517527.2	4	871	XP_011515829.1
	XM_017013404.1	3	1093	XP_016868893.1
	XM_017013405.1	4	871	XP_016868894.1
	AY534247.1	4	876	AAT07096.1
	BC137104.1	4	794
	BC137105.1	4	730

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3572810	Chr.8:70694948 - 70719832 on Build GRCh38	Loss	XKR9
esv3576585	Chr.8:70645369 - 70750875 on Build GRCh38	Gain	LACTB2-AS1 XKR9 LACTB2
esv2761435	Chr.8:70702440 - 70719635 on Build GRCh38	Loss	XKR9
esv3617571	Chr.8:70700793 - 70719964 on Build GRCh38	Loss	XKR9

More Information

Additional Information:

For this assay, SNP(s) [rs112321073] 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