accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
See other LRRC56 CNV Assays ›
Gene Symbol
LRRC56
Assay Reference Genome
Location

Chr.11:528274 on build GRCh38
Cytoband
11p15.5
Assay ID Hs03795144_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 115399

Gene Name:

 leucine rich repeat containing 56

Gene Aliases:

 -

Location:

 Chr.11:518967-554916 on Build GRCh38

Assay Gene Location:

 Overlaps Exon 3 - Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LRRC56 XM_011519875.2 XP_011518177.1
XM_011519877.2 XP_011518179.1
XM_017017167.1 XP_016872656.1
XM_017017168.1 XP_016872657.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv467634 Chr.11:511805 - 619789 on Build GRCh38 Loss HRAS MIR210 PHRF1 MIR210HG LOC143666 LMNTD2 LOC101059906 LRRC56 RASSF7 IRF7 CDHR5
nsv527327 Chr.11:295343 - 620599 on Build GRCh38 Loss RNH1 HRAS SIGIRR PHRF1 MIR210HG B4GALNT4 LOC143666 LRRC56 PKP3 IFITM3 IFITM1 IFITM2 RASSF7 CDHR5 MIR210 ANO9 LMNTD2 PTDSS2 LOC101059906 IFITM5 PGGHG IRF7
nsv469923 Chr.11:378188 - 1302334 on Build GRCh38 Loss LOC101927503 HRAS SIGIRR SNORA52 MUC5B MIR210HG B4GALNT4 PKP3 RASSF7 CDHR5 PANO1 MIR210 PIDD1 ANO9 CEND1 TOLLIP TMEM80 DEAF1 SCT LOC101059906 SLC25A22 CRACR2B DRD4 RNH1 EPS8L2 PHRF1 TALDO1 AP2A2 RPLP2 LOC143666 PDDC1 MUC6 MIR6744 LRRC56 TSPAN4 CD151 MUC2 PNPLA2 MUC5AC LOC171391 CHID1 LMNTD2 PTDSS2 POLR2L IRF7
esv2759794 Chr.11:409846 - 1336162 on Build GRCh38 Loss LOC101927503 HRAS SIGIRR SNORA52 MUC5B MIR210HG RASSF7 CDHR5 PANO1 MIR210 PIDD1 ANO9 CEND1 TOLLIP TMEM80 DEAF1 SCT LOC101059906 SLC25A22 CRACR2B DRD4 RNH1 EPS8L2 PHRF1 TALDO1 AP2A2 RPLP2 LOC143666 PDDC1 MUC6 MIR6744 LRRC56 TSPAN4 CD151 MUC2 PNPLA2 MUC5AC LOC171391 CHID1 TOLLIP-AS1 LMNTD2 PTDSS2 POLR2L IRF7
esv3366265 Chr.11:528252 - 531250 on Build GRCh38 Duplication LOC101059906 LRRC56
nsv1053964 Chr.11:491334 - 692433 on Build GRCh38 Gain DRD4 RNH1 HRAS PHRF1 MIR210HG LOC143666 LRRC56 RASSF7 CDHR5 MIR210 LMNTD2 DEAF1 PTDSS2 SCT LOC101059906 IRF7
dgv182e199 Chr.11:349830 - 943372 on Build GRCh38 Deletion HRAS SIGIRR SNORA52 MIR210HG B4GALNT4 PKP3 RASSF7 CDHR5 PANO1 MIR210 PIDD1 ANO9 CEND1 TMEM80 DEAF1 SCT LOC101059906 SLC25A22 CRACR2B DRD4 RNH1 EPS8L2 PHRF1 TALDO1 AP2A2 RPLP2 LOC143666 PDDC1 LRRC56 TSPAN4 CD151 PNPLA2 LOC171391 CHID1 LMNTD2 PTDSS2 POLR2L IRF7
nsv1159791 Chr.11:461793 - 909492 on Build GRCh38 Deletion HRAS SNORA52 MIR210HG RASSF7 CDHR5 PANO1 MIR210 PIDD1 CEND1 TMEM80 DEAF1 SCT LOC101059906 SLC25A22 CRACR2B DRD4 RNH1 EPS8L2 PHRF1 TALDO1 RPLP2 LOC143666 PDDC1 LRRC56 TSPAN4 CD151 PNPLA2 LOC171391 CHID1 LMNTD2 PTDSS2 POLR2L IRF7

Back To Top

More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

Back To Top

Related Products