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See other BCL2L11 CNV Assays ›
Gene Symbol
BCL2L11
Assay Reference Genome
Location

Chr.2:111123776 on build GRCh38
Cytoband
2q13
Assay ID Hs01692399_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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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 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
BCL2L11 NM_001204106.1 2 319 NP_001191035.1
NM_001204107.1 2 319 NP_001191036.1
NM_001204108.1 2 319 NP_001191037.1
NM_001204109.1 2 319 NP_001191038.1
NM_001204110.1 2 319 NP_001191039.1
NM_001204111.1 2 319 NP_001191040.1
NM_001204112.1 2 319 NP_001191041.1
NM_001204113.1 2 319 NP_001191042.1
NM_006538.4 2 319 NP_006529.1
NM_138621.4 2 319 NP_619527.1
NM_138622.3 2 319 NP_619528.1
NM_138623.3 2 319 NP_619529.1
NM_138624.3 2 319 NP_619530.1
NM_138625.3 2 319 NP_619531.1
NM_138626.3 2 319 NP_619532.1
NM_138627.3 2 319 NP_619533.1
NM_207002.3 2 319 NP_996885.1
NM_207003.2 2 319 NP_996886.1
XM_005263550.3 2 1097 XP_005263607.1
XM_005263551.2 2 1097 XP_005263608.1
XM_005263552.3 2 1097 XP_005263609.1
XM_005263553.2 2 1097 XP_005263610.1
XM_005263554.2 2 1097 XP_005263611.1
XM_005263555.3 2 1097 XP_005263612.1
XM_005263556.3 2 319 XP_005263613.1
XM_005263557.4 2 396 XP_005263614.1
XM_005263559.2 2 1097 XP_005263616.1
XM_005263561.3 2 319 XP_005263618.1
XM_011510461.2 2 1097 XP_011508763.1
XM_011510464.2 2 1097 XP_011508766.1
XM_017003101.1 2 1097 XP_016858590.1
XM_017003102.1 2 319 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 2 319
AK291269.1 2 316
AW629314.1
AY305714.1 AAQ82546.1
AY305715.1 AAQ82547.1
AY305716.1 AAT34900.1
AY352518.1 AAQ62569.1
AY423441.1 AAQ99148.1
AY423442.1 AAQ99149.1
AY423443.1 AAQ99150.1
AY428962.1 AAR06908.1
BC033694.1 2 301 AAH33694.1
CN411912.1 2 288
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
nsv829618 Chr.2:111118050 - 111123970 on Build GRCh38 Gain ACOXL BCL2L11
nsv582699 Chr.2:110763166 - 112172487 on Build GRCh38 Loss LOC400997 ANAPC1 MIR4771-2 TMEM87B FBLN7 MIR4435-2HG MERTK MIR4435-2 ACOXL PAFAH1B1P2 BCL2L11
nsv521956 Chr.2:110634682 - 112341235 on Build GRCh38 Loss LOC400997 ANAPC1 SNORD132 MIR4771-2 TMEM87B FBLN7 ZC3H8 MIR4435-2 BCL2L11 MIR4435-2HG BUB1 MERTK ZC3H6 ACOXL PAFAH1B1P2
nsv834331 Chr.2:111054562 - 111247101 on Build GRCh38 Loss LOC400997 MIR4435-2HG ACOXL BCL2L11
dgv4047n100 Chr.2:110308696 - 112358403 on Build GRCh38 Loss LINC01106 LOC400997 ANAPC1 SNORD132 MIR4771-2 TMEM87B FBLN7 ZC3H8 RGPD6 MIR4435-2 BCL2L11 LOC105375809 LIMS4 MIR4435-2HG BUB1 MERTK LOC100288570 LOC105373553 ZC3H6 ACOXL PAFAH1B1P2

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)


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