Hs06932358_cn

• Gene Symbol: TM7SF3
• Assay Reference Genome Location: Chr.12:26970178 on build GRCh38
• Cytoband: 12p11.23

Target Gene Details

• Entrez Gene ID: 51768
• Gene Name: transmembrane 7 superfamily member 3
• Gene Aliases: -
• Location: Chr.12:26966519-27014427 on Build GRCh38
• Assay Gene Location: Within Exon 13

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TM7SF3	XM_005253391.3	11	5606	XP_005253448.1
	XM_011520690.2	11	5601	XP_011518992.1
	XM_017019463.1	12	5849	XP_016874952.1
	XM_017019464.1	10	5411	XP_016874953.1
	XM_017019465.1	9	5258	XP_016874954.1
	XM_017019466.1	10	5425	XP_016874955.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3892165	Chr.12:26965680 - 26971722 on Build GRCh38	Loss	FGFR1OP2 TM7SF3
esv3892164	Chr.12:26945269 - 26971722 on Build GRCh38	Loss	FGFR1OP2 TM7SF3

More Information

Additional Information:

For this assay, SNP(s) [rs112936580] 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)

biological_process

Function(s)

molecular_function