Hs02746924_cn

• Gene Symbol: SLC10A5
• Assay Reference Genome Location: Chr.8:81694799 on build GRCh38
• Cytoband: 8q21.13

Target Gene Details

• Entrez Gene ID: 347051
• Gene Name: solute carrier family 10 member 5
• Gene Aliases: P5
• Location: Chr.8:81693656-81694972 on Build GRCh38
• Assay Gene Location: Within Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLC10A5	NM_001010893.2	1	174	NP_001010893.1
	AK095808.1	1	1376
	AY825924.1	1	174	AAV80707.1
	BC136625.1	1	254
	BC136631.1	1	254

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv611607	Chr.8:81405621 - 81768032 on Build GRCh38	Gain	FABP9 FABP4 FABP12 CHMP4C SLC10A5 IMPA1 PMP2 ZFAND1
nsv831369	Chr.8:81605833 - 81823586 on Build GRCh38	Gain+Loss	SNX16 CHMP4C SLC10A5 IMPA1 ZFAND1
nsv831368	Chr.8:81554926 - 81697395 on Build GRCh38	Gain	FABP12 SLC10A5 IMPA1

More Information

Additional Information:

For this assay, SNP(s) [rs78323957] 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

Panther Classification:

Molecular Function -

primary active transporter

Gene Ontology Categories:

Process(es)

sodium ion transport
bile acid and bile salt transport
transmembrane transport

Function(s)

bile acid:sodium symporter activity