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See other LMNTD2 CNV Assays ›
Gene Symbol
LMNTD2
Assay Reference Genome
Location

Chr.11:555894 on build GRCh38
Cytoband
11p15.5
Assay ID Hs02825360_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 256329

Gene Name:

 lamin tail domain containing 2

Gene Aliases:

 C11orf35

Location:

 Chr.11:554850-560780 on Build GRCh38

Assay Gene Location:

 Within Exon 12
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LMNTD2 NM_173573.2 NP_775844.2
XM_011519965.2 XP_011518267.2
XM_011519967.2 XP_011518269.2
XM_017017476.1 11 1717 XP_016872965.1
XM_017017477.1 11 1702 XP_016872966.1
XM_017017478.1 11 1558 XP_016872967.1
XM_017017479.1 XP_016872968.1
AI539379.1
BC039077.1 AAH39077.1
BX384084.2

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv552854 Chr.11:511805 - 619789 on Build GRCh38 Loss HRAS RASSF7 CDHR5 LOC101059906 LOC143666 LMNTD2 MIR210HG PHRF1 LRRC56 IRF7 MIR210
nsv527327 Chr.11:295343 - 620599 on Build GRCh38 Loss PKP3 RASSF7 ANO9 IFITM3 CDHR5 LMNTD2 PGGHG IFITM2 SIGIRR PTDSS2 MIR210HG PHRF1 MIR210 HRAS B4GALNT4 IFITM1 LOC101059906 LOC143666 IFITM5 RNH1 LRRC56 IRF7
nsv951270 Chr.11:528401 - 628100 on Build GRCh38 Deletion HRAS RASSF7 CDHR5 LOC101059906 LOC143666 LMNTD2 SCT MIR210HG PHRF1 LRRC56 IRF7 MIR210
nsv469923 Chr.11:378188 - 1302334 on Build GRCh38 Loss PKP3 DRD4 RASSF7 MUC5B ANO9 CRACR2B CDHR5 PNPLA2 LMNTD2 CD151 SIGIRR TOLLIP SNORA52 B4GALNT4 RPLP2 POLR2L PDDC1 MUC5AC LRRC56 PANO1 IRF7 DEAF1 CEND1 TALDO1 EPS8L2 LOC171391 TSPAN4 CHID1 LOC101927503 PTDSS2 MIR210HG PHRF1 MIR210 HRAS TMEM80 AP2A2 PIDD1 SLC25A22 MUC2 MUC6 LOC101059906 LOC143666 SCT RNH1 MIR6744
esv3625070 Chr.11:553728 - 559392 on Build GRCh38 Loss LMNTD2 LRRC56
esv2759794 Chr.11:409846 - 1336162 on Build GRCh38 Loss DRD4 RASSF7 MUC5B ANO9 CRACR2B CDHR5 PNPLA2 LMNTD2 CD151 SIGIRR TOLLIP-AS1 TOLLIP SNORA52 RPLP2 POLR2L PDDC1 MUC5AC LRRC56 PANO1 IRF7 DEAF1 CEND1 TALDO1 EPS8L2 LOC171391 TSPAN4 CHID1 LOC101927503 PTDSS2 MIR210HG PHRF1 MIR210 HRAS TMEM80 AP2A2 PIDD1 SLC25A22 MUC2 MUC6 LOC101059906 LOC143666 SCT RNH1 MIR6744
nsv1039558 Chr.11:534242 - 672091 on Build GRCh38 Gain DRD4 RASSF7 CDHR5 LMNTD2 MIR210HG PHRF1 MIR210 HRAS LOC143666 SCT LRRC56 IRF7 DEAF1
dgv182e199 Chr.11:349830 - 943372 on Build GRCh38 Deletion PKP3 DRD4 RASSF7 ANO9 CRACR2B CDHR5 PNPLA2 LMNTD2 CD151 SIGIRR SNORA52 B4GALNT4 RPLP2 POLR2L PDDC1 LRRC56 PANO1 IRF7 DEAF1 CEND1 TALDO1 EPS8L2 LOC171391 TSPAN4 CHID1 PTDSS2 MIR210HG PHRF1 MIR210 HRAS TMEM80 AP2A2 PIDD1 SLC25A22 LOC101059906 LOC143666 SCT RNH1
nsv1053964 Chr.11:491334 - 692433 on Build GRCh38 Gain DRD4 RASSF7 CDHR5 LMNTD2 PTDSS2 MIR210HG PHRF1 MIR210 HRAS LOC101059906 LOC143666 SCT RNH1 LRRC56 IRF7 DEAF1
nsv1159791 Chr.11:461793 - 909492 on Build GRCh38 Deletion DRD4 RASSF7 CRACR2B CDHR5 PNPLA2 LMNTD2 CD151 SNORA52 RPLP2 POLR2L PDDC1 LRRC56 PANO1 IRF7 DEAF1 CEND1 TALDO1 EPS8L2 LOC171391 TSPAN4 CHID1 PTDSS2 MIR210HG PHRF1 MIR210 HRAS TMEM80 PIDD1 SLC25A22 LOC101059906 LOC143666 SCT RNH1
nsv469924 Chr.11:549119 - 609887 on Build GRCh38 Gain RASSF7 LOC143666 LMNTD2 MIR210HG PHRF1 LRRC56 MIR210

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

Gene Ontology Categories:

Function(s)


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