Hs01798627_cn

• Gene Symbol: SLC9B2
• Assay Reference Genome Location: Chr.4:103026374 on build GRCh38
• Cytoband: 4q24

Target Gene Details

• Entrez Gene ID: 133308
• Gene Name: solute carrier family 9 member B2
• Gene Aliases: NHA2, NHE10, NHEDC2
• Location: Chr.4:103018033-103077371 on Build GRCh38
• Assay Gene Location: Within Exon 13

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLC9B2	NM_001300754.1	11	1705	NP_001287683.1
	NM_001300756.1	10	1934	NP_001287685.1
	NM_178833.5	12	2242	NP_849155.2
	XM_006714085.2			XP_006714148.1
	XM_006714086.3	11	2070	XP_006714149.1
	AA233228.1	2	326
	AK172823.1	12	2242	BAD18790.1
	AK297010.1	11	1616
	AK299888.1
	BC009732.1			AAH09732.1
	BC047447.1			AAH47447.2
	BI962996.1	1	106
	BX359760.2	1	842

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv4445	Chr.4:103003411 - 103034963 on Build GRCh38	Insertion	SLC9B1 SLC9B2
nsv461598	Chr.4:102886563 - 103032232 on Build GRCh38	Loss	SLC9B1 CISD2 SLC9B2
nsv830021	Chr.4:103013297 - 103179431 on Build GRCh38	Loss	BDH2 SLC9B1 CENPE SLC9B2
esv2759270	Chr.4:102859548 - 103136164 on Build GRCh38	Gain	BDH2 UBE2D3 SLC9B1 CISD2 CENPE SLC9B2

More Information

Additional Information:

For this assay, SNP(s) [rs111508094] 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)

sodium ion transport
ion transmembrane transport
hydrogen ion transmembrane transport
positive regulation of osteoclast development

Function(s)

monovalent cation:proton antiporter activity