Hs00226062_cn

• Gene Symbol: SLC2A7
• Assay Reference Genome Location: Chr.1:9014848 on build GRCh38
• Cytoband: 1p36.23

Target Gene Details

• Entrez Gene ID: 155184
• Gene Name: solute carrier family 2 member 7
• Gene Aliases: GLUT7
• Location: Chr.1:8992534-9026384 on Build GRCh38
• Assay Gene Location: Overlaps Intron 6 - Exon 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
SLC2A7	NM_207420.2			NP_997303.2
	XM_011540824.2			XP_011539126.1
	XM_011540825.2			XP_011539127.1
	AY571960.2

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv545345	Chr.1:8831066 - 9035551 on Build GRCh38	Gain	MIR6728 CA6 ENO1 SLC2A7 ENO1-AS1
nsv1004025	Chr.1:9000983 - 9069086 on Build GRCh38	Gain	SLC2A7 SLC2A5
nsv525092	Chr.1:8998487 - 9020907 on Build GRCh38	Gain	SLC2A7
dgv15n100	Chr.1:8992095 - 9056684 on Build GRCh38	Loss	SLC2A7 SLC2A5

More Information

Additional Information:

For this assay, SNP(s) [rs78914166] 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, Non-exonic, DGV Variation

Gene Ontology Categories:

Process(es)

carbohydrate transmembrane transport

Function(s)

sugar transmembrane transporter activity