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System Message

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Gene Symbol: BCL2L11
Assay Reference Genome Location: Chr.2:111150601 on build GRCh38
Cytoband: 2q13

Assay ID

Hs04620441_cn

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Availability	Made To Order
Catalog #	4400291
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Genomic Map
Assay Details
More Information

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 Exon 10

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	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_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	3	2018	XP_005263607.1
	XM_005263551.2			XP_005263608.1
	XM_005263552.3	4	1838	XP_005263609.1
	XM_005263553.2			XP_005263610.1
	XM_005263554.2			XP_005263611.1
	XM_005263555.3	3	1748	XP_005263612.1
	XM_005263556.3	3	1240	XP_005263613.1
	XM_005263557.4	3	1317	XP_005263614.1
	XM_005263559.2			XP_005263616.1
	XM_005263561.3	4	1060	XP_005263618.1
	XM_017003101.1			XP_016858590.1
	XM_017003102.1	3	970	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
	AF455755.1	1	653	AAL57868.1
	AK290377.1
	AK291269.1
	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
nsv521956	Chr.2:110634682 - 112341235 on Build GRCh38	Loss	TMEM87B LOC400997 ZC3H6 MIR4435-2HG MIR4435-2 BUB1 BCL2L11 ANAPC1 ZC3H8 SNORD132 FBLN7 PAFAH1B1P2 MERTK MIR4771-2 ACOXL
nsv582699	Chr.2:110763166 - 112172487 on Build GRCh38	Loss	FBLN7 TMEM87B LOC400997 MIR4435-2HG PAFAH1B1P2 MIR4435-2 BCL2L11 ANAPC1 MERTK MIR4771-2 ACOXL
nsv834331	Chr.2:111054562 - 111247101 on Build GRCh38	Loss	LOC400997 MIR4435-2HG BCL2L11 ACOXL
esv2759083	Chr.2:111142206 - 111989360 on Build GRCh38	Gain+Loss	MIR4435-2HG PAFAH1B1P2 MIR4435-2 BCL2L11 ANAPC1 MERTK MIR4771-2
dgv4047n100	Chr.2:110308696 - 112358403 on Build GRCh38	Loss	TMEM87B LOC400997 RGPD6 ZC3H6 MIR4435-2HG LOC100288570 MIR4435-2 BUB1 BCL2L11 ANAPC1 ZC3H8 LOC105373553 LINC01106 SNORD132 FBLN7 LIMS4 PAFAH1B1P2 MERTK LOC105375809 MIR4771-2 ACOXL

More Information

Set Membership:

Intragenic

Exonic

DGV Variation

Gene Ontology Categories:

Function(s) Process(es)

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