Genomic Map

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Assay Details

Target Gene Details

Entrez Gene ID:	284525
Gene Name:	solute carrier family 9 member C2 (putative)
Gene Aliases:	SLC9A11
Location:	Chr.1:173500465-173603094 on Build GRCh38
Assay Gene Location:	Within Exon 29

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLC9C2	NM_178527.3	28	4100	NP_848622.2
	XM_011509426.1	29	4138	XP_011507728.1
	XM_017001065.1	29	3833	XP_016856554.1
	XM_017001066.1	29	3827	XP_016856555.1
	XM_017001067.1	28	4018	XP_016856556.1
	XM_017001068.1	28	4037	XP_016856557.1
	XM_017001069.1	28	3732	XP_016856558.1
	XM_017001070.1	28	3726	XP_016856559.1
	XM_017001071.1	29	3745	XP_016856560.1
	XM_017001072.1	27	3871	XP_016856561.1
	XM_017001073.1	28	3644	XP_016856562.1
	XM_017001074.1	27	3573	XP_016856563.1
	XM_017001075.1	22	2900	XP_016856564.1
	XM_017001076.1	19	2507	XP_016856565.1
	AK128104.1	28	4100
	BC042592.1	28	4047	AAH42592.1
	BX648119.1	21	3011

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv831915	Chr.1:173299285 - 173513018 on Build GRCh38	Gain+Loss	SLC9C2 LOC100506023 LOC101928673 PRDX6 TNFSF4

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More Information

Additional Information:

For this assay, SNP(s) [rs114708311] 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.