Hs06874823_cn

• Gene Symbol: LINGO2
• Assay Reference Genome Location: Chr.9:27941952 on build GRCh38
• Cytoband: 9p21.2

Target Gene Details

• Entrez Gene ID: 158038
• Gene Name: leucine rich repeat and Ig domain containing 2
• Gene Aliases: LERN3, LRRN6C
• Location: Chr.9:27937617-29213981 on Build GRCh38
• Assay Gene Location: Within Exon 15

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LINGO2	XM_011517719.1	6	10238	XP_011516021.1
	XM_011517724.2	5	13257	XP_011516026.1
	XM_011517728.2	2	13036	XP_011516030.1
	XM_017014303.1	11	13141	XP_016869792.1
	XM_017014304.1	4	15661	XP_016869793.1
	XM_017014305.1	5	15244	XP_016869794.1
	XM_017014306.1	3	12405	XP_016869795.1
	XM_017014307.1	2	9878	XP_016869796.1
	BX538226.1	1	2546

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv613950	Chr.9:27746787 - 28342181 on Build GRCh38	Gain	LOC646700 LINGO2

More Information

Additional Information:

For this assay, SNP(s) [rs75385167] 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

Panther Classification:

Molecular Function -

transmembrane signal receptor

Gene Ontology Categories:

Process(es)

axonogenesis
positive regulation of synapse assembly