Hs03628466_cn

• Gene Symbol: BRI3
• Assay Reference Genome Location: Chr.7:98290909 on build GRCh38
• Cytoband: 7q21.3

Target Gene Details

• Entrez Gene ID: 25798
• Gene Name: brain protein I3
• Gene Aliases: I3
• Location: Chr.7:98281667-98322398 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
BRI3	NM_001159491.1			NP_001152963.1
	NM_015379.4			NP_056194.1
	XM_017011931.1			XP_016867420.1
	XM_017011932.1			XP_016867421.1
	XM_017011933.1			XP_016867422.1
	XM_017011934.1			XP_016867423.1
	XM_017011935.1			XP_016867424.1
	XM_017011936.1			XP_016867425.1
	AB055977.1			BAB32785.1
	AF041430.2			AAF18565.2
	AF106966.1			AAD05167.1
	BC018737.1			AAH18737.1
	BC062370.1			AAH62370.1
	BF108440.1
	BF432881.1
	BQ018487.1
	CB054862.1
	CB528682.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv831067	Chr.7:98230857 - 98436216 on Build GRCh38	Loss	TECPR1 BAIAP2L1 BRI3

More Information

Additional Information:

For this assay, SNP(s) [rs78257253] 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, Intronic, Non-exonic, DGV Variation

Gene Ontology Categories:

Function(s)

identical protein binding