Hs06632644_cn

• Gene Symbol: ESYT3
• Assay Reference Genome Location: Chr.3:138444039 on build GRCh38
• Cytoband: 3q22.3

Target Gene Details

• Entrez Gene ID: 83850
• Gene Name: extended synaptotagmin 3
• Gene Aliases: CHR3SYT, E-Syt3, FAM62C
• Location: Chr.3:138434573-138479942 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ESYT3	NM_001322831.1			NP_001309760.1
	NM_001322834.1			NP_001309763.1
	NM_031913.4			NP_114119.2
	NR_136409.1
	AK125080.1
	AK289530.1
	DQ993202.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv999041	Chr.3:138429970 - 138629146 on Build GRCh38	Gain	CEP70 FAIM ESYT3
nsv428422	Chr.3:137344347 - 138686784 on Build GRCh38	Gain+Loss	CEP70 DBR1 ARMC8 FAIM MRAS PIK3CB DZIP1L A4GNT SOX14 CLDN18 NME9 ESYT3 LINC01210
nsv591853	Chr.3:138381697 - 138475593 on Build GRCh38	Loss	ESYT3 MRAS

More Information

Additional Information:

For this assay, SNP(s) [rs116492611] 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:

Process(es)

lipid transport

Function(s)

protein binding
lipid binding
metal ion binding