Hs01625337_cn

• Gene Symbol: APBB3
• Assay Reference Genome Location: Chr.5:140558608 on build GRCh38
• Cytoband: 5q31.3

Target Gene Details

• Entrez Gene ID: 10307
• Gene Name: amyloid beta precursor protein binding family B member 3
• Gene Aliases: FE65L2, SRA
• Location: Chr.5:140558268-140564604 on Build GRCh38
• Assay Gene Location: Within Exon 13

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
APBB3	NM_006051.3	13	1818	NP_006042.3
	NM_133172.2	12	1812	NP_573418.2
	NM_133173.2	13	1797	NP_573419.2
	NM_133174.2	12	1791	NP_573420.2
	AB018247.1	13	1489	BAA35188.1
	AB049618.1	13	1681	BAB40806.1
	AB061224.1			BAB71767.1
	AB094990.1			BAC22578.1
	AB209839.1	13	1525	BAD93076.1
	AF224708.1	12	1473	AAF65172.1
	AF224709.1	13	1458	AAF65173.1
	AF224710.1	12	1452	AAF65174.1
	AF224711.1	13	1479	AAF65175.1
	AK074885.1	8	1724
	AK075280.1	13	1760
	AK125244.1	10	2450
	AK304824.1	9	1818
	BC013158.1	13	1797	AAH13158.1
	BC125187.1	13	1789
	BF448559.1	1	350

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv599825	Chr.5:140556654 - 140626201 on Build GRCh38	Loss	SLC35A4 SRA1 MIR6831 APBB3 TMCO6

More Information

Additional Information:

For this assay, SNP(s) [rs145698446] 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)

regulation of transcription, DNA-templated

Function(s)

beta-amyloid binding
protein binding
transcription factor binding