Hs06103822_cn

• Gene Symbol: N4BP3
• Assay Reference Genome Location: Chr.5:178113858 on build GRCh38
• Cytoband: 5q35.3

Target Gene Details

• Entrez Gene ID: 23138
• Gene Name: NEDD4 binding protein 3
• Gene Aliases: LZTS4
• Location: Chr.5:178113506-178127034 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
N4BP3	NM_015111.1			NP_055926.1
	XM_006714834.3			XP_006714897.1
	XM_011534473.1			XP_011532775.1
	XM_011534474.1			XP_011532776.1
	BC053323.1			AAH53323.2

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1019404	Chr.5:178080079 - 178432088 on Build GRCh38	Gain	COL23A1 RMND5B GMCL1P1 HNRNPAB NHP2 PHYKPL N4BP3
nsv462567	Chr.5:178078020 - 178145926 on Build GRCh38	Loss	RMND5B N4BP3
dgv5844n100	Chr.5:177883324 - 178184647 on Build GRCh38	Gain	RMND5B LOC100288656 GMCL1P1 LOC728554 FAM153C LOC100128340 NHP2 N4BP3 PROP1
nsv1144125	Chr.5:178113499 - 178113899 on Build GRCh38	Deletion	N4BP3
nsv950730	Chr.5:178113500 - 178114599 on Build GRCh38	Deletion	N4BP3
nsv600391	Chr.5:178061280 - 178122490 on Build GRCh38	Loss	N4BP3

More Information

Additional Information:

For this assay, SNP(s) [rs73348171] 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