Hs05366126_cn

• Gene Symbol: TLN2
• Assay Reference Genome Location: Chr.15:62417690 on build GRCh38
• Cytoband: 15q22.2

Target Gene Details

• Entrez Gene ID: 83660
• Gene Name: talin 2
• Gene Aliases: ILWEQ
• Location: Chr.15:62390527-62844631 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
TLN2	XM_005254708.4			XP_005254765.1
	XM_005254710.4			XP_005254767.1
	XM_005254711.4			XP_005254768.1
	XM_005254714.3			XP_005254771.1
	AB621808.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv4567n54	Chr.15:62413995 - 62428164 on Build GRCh38	Loss	TLN2
nsv833031	Chr.15:62330187 - 62509069 on Build GRCh38	Loss	TLN2 MIR6085
nsv1035441	Chr.15:62406037 - 63349997 on Build GRCh38	Gain	LOC105370854 LACTB APH1B TLN2 MGC15885 MIR190A LOC101928955 TPM1 CA12 RAB8B RPS27L

More Information

Additional Information:

For this assay, SNP(s) [rs114060130] 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)

cytoskeletal anchoring at plasma membrane
cell-cell junction assembly
cell adhesion

Function(s)

actin binding
structural molecule activity
structural constituent of cytoskeleton
protein binding
actin filament binding