Hs06930038_cn

• Gene Symbol: BCL2L14
• Assay Reference Genome Location: Chr.12:12084655 on build GRCh38
• Cytoband: 12p13.2

Target Gene Details

• Entrez Gene ID: 79370
• Gene Name: BCL2 like 14
• Gene Aliases: BCLG
• Location: Chr.12:12049844-12099695 on Build GRCh38
• Assay Gene Location: Within Intron 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
BCL2L14	NM_030766.1			NP_110393.1
	NM_138722.1			NP_620048.1
	NM_138723.1			NP_620049.1
	XM_006719151.3			XP_006719214.1
	XM_011520848.1			XP_011519150.1
	XM_011520849.1			XP_011519151.1
	XM_017019963.1			XP_016875452.1
	AF281254.1			AAG59793.1
	AF281255.1			AAG59794.1
	AK223415.1			BAD97135.1
	AK292995.1
	AY040274.1			AAK72109.1
	BC025778.1			AAH25778.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1046355	Chr.12:11501836 - 12890185 on Build GRCh38	Loss	MIR613 DDX47 GPR19 CREBL2 DUSP16 ETV6 LINC01252 RPL13AP20 MIR1244-4 LOC105369662 CDKN1B APOLD1 LOC100506248 LOH12CR2 BCL2L14 LRP6 BORCS5 MANSC1

More Information

Additional Information:

For this assay, SNP(s) [rs74064616] 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)

apoptotic process
regulation of apoptotic process

Function(s)

protein binding
protein kinase binding