Hs05822117_cn

• Gene Symbol: LOC101928161
• Assay Reference Genome Location: Chr.2:133275427 on build GRCh38
• Cytoband: 2q21.2

Target Gene Details

• Entrez Gene ID: 101928161
• Gene Name: uncharacterized LOC101928161
• Gene Aliases: -
• Location: Chr.2:133266195-133284758 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC101928161	NR_110294.1
	DB498836.1

Target Gene Details

• Entrez Gene ID: 344148
• Gene Name: NCK associated protein 5
• Gene Aliases: ERIH1, ERIH2, NAP5
• Location: Chr.2:132671788-133675181 on Build GRCh38
• Assay Gene Location: Within Intron 11

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
NCKAP5	NM_207363.2			NP_997246.2
	NM_207481.3			NP_997364.3
	XM_005263659.3			XP_005263716.1
	XM_005263660.3			XP_005263717.1
	XM_011511097.2			XP_011509399.1
	XM_011511098.2			XP_011509400.1
	XM_011511099.2			XP_011509401.1
	XM_011511100.2			XP_011509402.1
	XM_011511101.1			XP_011509403.1
	XM_011511102.2			XP_011509404.1
	XM_011511104.1			XP_011509406.1
	XM_017003974.1			XP_016859463.1
	XM_017003975.1			XP_016859464.1
	XM_017003976.1			XP_016859465.1
	XM_017003977.1			XP_016859466.1
	XM_017003979.1			XP_016859468.1
	AK057980.1
	AK092189.1			BAC03824.1
	BC110831.1			AAI10832.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv516915	Chr.2:133242259 - 133297090 on Build GRCh38	Gain	LOC101928161 NCKAP5
nsv1011100	Chr.2:133142490 - 133288591 on Build GRCh38	Loss	LOC101928161 NCKAP5
nsv583152	Chr.2:132369502 - 133631550 on Build GRCh38	Gain	LOC101928161 NCKAP5 GPR39 LOC101928185 LYPD1
nsv2933	Chr.2:133248612 - 133282407 on Build GRCh38	Insertion	LOC101928161 NCKAP5
nsv834384	Chr.2:133247657 - 133431077 on Build GRCh38	Gain	LOC101928161 NCKAP5
esv3893403	Chr.2:133198640 - 133353352 on Build GRCh38	Loss	LOC101928161 NCKAP5

More Information

Additional Information:

For this assay, SNP(s) [rs144494068] 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)

biological_process