Assay Details

Target Gene Details

Entrez Gene ID:	10018
Gene Name:	BCL2 like 11
Gene Aliases:	BAM, BIM, BOD
Location:	Chr.2:111120914-111168445 on Build GRCh38
Assay Gene Location:	Within Intron 6

Gene Symbol	Transcript Accession	Protein ID
BCL2L11	NM_001204106.1	NP_001191035.1
	NM_001204107.1	NP_001191036.1
	NM_001204108.1	NP_001191037.1
	NM_001204109.1	NP_001191038.1
	NM_001204110.1	NP_001191039.1
	NM_001204111.1	NP_001191040.1
	NM_001204112.1	NP_001191041.1
	NM_001204113.1	NP_001191042.1
	NM_006538.4	NP_006529.1
	NM_138621.4	NP_619527.1
	NM_138622.3	NP_619528.1
	NM_138623.3	NP_619529.1
	NM_138624.3	NP_619530.1
	NM_138625.3	NP_619531.1
	NM_138626.3	NP_619532.1
	NM_138627.3	NP_619533.1
	NM_207003.2	NP_996886.1
	XM_005263550.3	XP_005263607.1
	XM_005263551.2	XP_005263608.1
	XM_005263552.3	XP_005263609.1
	XM_005263553.2	XP_005263610.1
	XM_005263554.2	XP_005263611.1
	XM_005263555.3	XP_005263612.1
	XM_005263556.3	XP_005263613.1
	XM_005263557.4	XP_005263614.1
	XM_005263559.2	XP_005263616.1
	XM_005263561.3	XP_005263618.1
	XM_017003101.1	XP_016858590.1
	XM_017003102.1	XP_016858591.1
	AB071195.1	BAB78589.1
	AB071196.1	BAB78590.1
	AB071197.1	BAB78591.1
	AB071198.1	BAB78592.1
	AB071199.1	BAB78593.1
	AB071200.1	BAB78594.1
	AF032457.1	AAC39593.1
	AF032458.1	AAC39594.1
	AK290377.1
	AK291269.1
	AW629314.1
	AY305714.1	AAQ82546.1
	AY305715.1	AAQ82547.1
	AY305716.1	AAT34900.1
	AY423441.1	AAQ99148.1
	AY423442.1	AAQ99149.1
	AY423443.1	AAQ99150.1
	AY428962.1	AAR06908.1
	BC033694.1	AAH33694.1
	DQ849200.1	ABI13589.1
	DQ849201.1	ABI13590.1
	DQ849202.1	ABI13591.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv582699	Chr.2:110763166 - 112172487 on Build GRCh38	Loss	PAFAH1B1P2 MIR4435-2 ANAPC1 FBLN7 MIR4435-2HG BCL2L11 LOC400997 ACOXL MERTK MIR4771-2 TMEM87B
nsv521956	Chr.2:110634682 - 112341235 on Build GRCh38	Loss	ZC3H6 BUB1 FBLN7 BCL2L11 LOC400997 ACOXL MIR4771-2 TMEM87B PAFAH1B1P2 SNORD132 MIR4435-2 ANAPC1 MIR4435-2HG ZC3H8 MERTK
nsv834331	Chr.2:111054562 - 111247101 on Build GRCh38	Loss	MIR4435-2HG BCL2L11 LOC400997 ACOXL
dgv4047n100	Chr.2:110308696 - 112358403 on Build GRCh38	Loss	LOC105375809 ZC3H6 LOC100288570 BUB1 FBLN7 RGPD6 BCL2L11 LOC400997 ACOXL MIR4771-2 LIMS4 TMEM87B PAFAH1B1P2 SNORD132 LOC105373553 MIR4435-2 ANAPC1 MIR4435-2HG ZC3H8 MERTK LINC01106

More Information

Additional Information:

For this assay, SNP(s) [rs72836352] 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:

Function(s) Process(es)

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Genomic Map

Assay Details

Target Gene Details

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Gene Name:

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