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See other LILRB2 CNV Assays ›
Gene Symbol
LILRB2
Assay Reference Genome
Location

Chr.19:54279864 on build GRCh38
Cytoband
19q13.42
Assay ID Hs01716748_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 10288

Gene Name:

 leukocyte immunoglobulin like receptor B2

Gene Aliases:

 CD85D, ILT-4, ILT4, LIR-2, LIR2, MIR-10, MIR10

Location:

 Chr.19:54273821-54281178 on Build GRCh38

Assay Gene Location:

 Within Exon 5
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LILRB2 NM_001080978.3 4 548 NP_001074447.2
NM_001278403.2 4 410 NP_001265332.2
NM_001278404.2 3 397 NP_001265333.2
NM_001278405.2 3 330 NP_001265334.2
NM_001278406.2 3 330 NP_001265335.2
NM_005874.4 4 548 NP_005865.3
NR_103521.2 3 414
AF000574.1 3 282 AAB88119.1
AF004231.2 4 410 AAB67711.1
AF011565.1 3 284 AAC51882.1
AF011566.1 3 284 AAC51883.1
AF025528.1 4 465 AAB87662.1
AF283986.1 4 456 AAL36990.1
AF283987.1 3 331 AAL36991.1
AK226015.1 4 521
AK297041.1 3 375
AK297071.1 4 503
AK298649.1 3 361
AK310263.1 3 360
BC036827.1 4 438 AAH36827.1
DC429031.1 3 414
DC429053.1 4 549
DQ655938.2
EU915606.1 3 282
LC125264.1 2 234

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv528370 Chr.19:54247206 - 54284902 on Build GRCh38 Loss MIR4752 LILRB2 LILRB5
dgv3654n100 Chr.19:54212959 - 54303818 on Build GRCh38 Gain MIR4752 LILRA6 LILRB2 LILRB3 LILRB5
esv2718860 Chr.19:54223005 - 54312746 on Build GRCh38 Deletion MIR4752 LILRA5 LILRA6 LILRB2 LILRB3 LILRB5
esv2718812 Chr.19:53184636 - 54322450 on Build GRCh38 Deletion MIR1283-2 MIR520C TMC4 ZNF525 MIR521-2 LOC284379 MIR520B ZNF845 VN1R4 MIR516A2 MIR519C MIR518A1 MIR523 LILRA5 LILRA6 MBOAT7 LILRB2 PRPF31 MIR518C MIR512-1 MIR519A1 TSEN34 ZNF331 BIRC8 TARM1 MIR518D VSTM1 MIR522 ZNF677 MIR1323 MIR526A1 MIR525 MIR519E MIR519A2 ZNF765 NDUFA3 MIR498 MIR517A MIR518E FAM90A27P MIR527 MIR371A ZNF818P CACNG8 ZNF813 MIR519B OSCAR MIR524 MIR515-1 LOC105372457 MIR521-1 MIR526A2 MIR516B1 MIR516B2 CACNG6 MIR372 LENG1 TPM3P9 MIR516A1 MIR515-2 MIR1283-1 MIR371B MIR373 MIR519D MIR4752 MIR520D MIR520G MIR526B LILRB5 MIR520F MIR517C MIR520A CACNG7 MIR518F VN1R2 ZNF761 MIR512-2 PRKCG RPS9 MIR517B MIR520E LILRB3 MIR935 MIR518A2 DPRX MIR520H ZNF665 TFPT MYADM CNOT3 MIR518B NLRP12
dgv3661n100 Chr.19:54249470 - 54336316 on Build GRCh38 Gain+Loss LILRA4 MIR4752 LILRA5 LILRB2 LILRB5
dgv3657n100 Chr.19:54215071 - 54282373 on Build GRCh38 Gain MIR4752 LILRA6 LILRB2 LILRB3 LILRB5
esv2758771 Chr.19:54163847 - 54954956 on Build GRCh38 Gain+Loss LENG9 TMC4 NLRP7 FCAR LENG8 LAIR1 KIR3DL3 LILRA1 MIR4752 LILRA5 LILRA6 MBOAT7 LILRB2 LILRB5 KIR2DL3 KIR2DL1 TSEN34 LILRA4 KIR3DX1 KIR3DL1 LOC102724300 LILRP2 LAIR2 KIR2DS4 RPS9 LILRB3 LILRB4 KIR2DL4 LILRB1 LOC101928804 NCR1 LENG8-AS1 KIR3DL2 MIR8061 TTYH1 CDC42EP5 LILRA2
dgv1074e212 Chr.19:54218859 - 54292176 on Build GRCh38 Gain MIR4752 LILRA6 LILRB2 LILRB3 LILRB5
esv2763032 Chr.19:54212971 - 54336316 on Build GRCh38 Gain+Loss LILRA4 MIR4752 LILRA5 LILRA6 LILRB2 LILRB3 LILRB5
esv3644793 Chr.19:54277904 - 54295912 on Build GRCh38 Gain MIR4752 LILRB2
dgv3660n100 Chr.19:54226329 - 54340836 on Build GRCh38 Gain LILRA4 MIR4752 LILRA5 LILRA6 LILRB2 LILRB5
nsv963078 Chr.19:54272549 - 54289938 on Build GRCh38 Duplication MIR4752 LILRB2
esv3574853 Chr.19:54226365 - 54326343 on Build GRCh38 Gain MIR4752 LILRA5 LILRA6 LILRB2 LILRB5
dgv6549n54 Chr.19:54219677 - 54336316 on Build GRCh38 Gain LILRA4 MIR4752 LILRA5 LILRA6 LILRB2 LILRB3 LILRB5
nsv580193 Chr.19:54227805 - 54284902 on Build GRCh38 Gain MIR4752 LILRA6 LILRB2 LILRB5
nsv833878 Chr.19:54268967 - 54518890 on Build GRCh38 Loss LENG9 LILRA4 LAIR2 MIR4752 LENG8-AS1 LILRA5 LILRB2 TTYH1 CDC42EP5 LENG8 LAIR1

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More Information


Additional Information:

For this assay, SNP(s) [rs73055442] 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 Exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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