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

Chr.11:558663 on build GRCh38
Cytoband
11p15.5
Assay ID Hs00931355_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 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LMNTD2 NM_173573.2 3 325 NP_775844.2
XM_011519965.2 3 485 XP_011518267.2
XM_011519967.2 3 485 XP_011518269.2
XM_017017476.1 3 485 XP_016872965.1
XM_017017477.1 3 485 XP_016872966.1
XM_017017478.1 3 326 XP_016872967.1
XM_017017479.1 3 485 XP_016872968.1
BC039077.1 3 325 AAH39077.1
BX384085.2 4 428

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 LOC143666 RASSF7 LOC101059906 CDHR5 MIR210HG MIR210 HRAS LMNTD2 IRF7 LRRC56 PHRF1
dgv1523n54 Chr.11:557342 - 656940 on Build GRCh38 Gain LOC143666 RASSF7 SCT CDHR5 DEAF1 MIR210HG MIR210 DRD4 LMNTD2 IRF7 PHRF1
nsv527327 Chr.11:295343 - 620599 on Build GRCh38 Loss ANO9 LOC143666 RASSF7 LOC101059906 IFITM1 B4GALNT4 MIR210HG MIR210 HRAS IRF7 PGGHG RNH1 IFITM2 PTDSS2 CDHR5 IFITM3 IFITM5 SIGIRR PKP3 LMNTD2 LRRC56 PHRF1
nsv951270 Chr.11:528401 - 628100 on Build GRCh38 Deletion LOC143666 RASSF7 LOC101059906 SCT CDHR5 MIR210HG MIR210 HRAS LMNTD2 IRF7 LRRC56 PHRF1
nsv469923 Chr.11:378188 - 1302334 on Build GRCh38 Loss LOC143666 TMEM80 LOC101927503 TALDO1 DEAF1 MIR210HG CHID1 AP2A2 EPS8L2 IRF7 MUC2 MUC6 RNH1 RPLP2 CDHR5 SIGIRR MIR6744 LMNTD2 PHRF1 PANO1 ANO9 RASSF7 PIDD1 LOC101059906 SCT CRACR2B B4GALNT4 MUC5AC LOC171391 POLR2L MIR210 HRAS PDDC1 PNPLA2 PTDSS2 SNORA52 MUC5B TSPAN4 CD151 CEND1 SLC25A22 DRD4 PKP3 LRRC56 TOLLIP
esv3625070 Chr.11:553728 - 559392 on Build GRCh38 Loss LMNTD2 LRRC56
esv2759794 Chr.11:409846 - 1336162 on Build GRCh38 Loss LOC143666 TMEM80 LOC101927503 TALDO1 DEAF1 MIR210HG CHID1 AP2A2 EPS8L2 IRF7 MUC2 MUC6 TOLLIP-AS1 RNH1 RPLP2 CDHR5 SIGIRR MIR6744 LMNTD2 PHRF1 PANO1 ANO9 RASSF7 PIDD1 LOC101059906 SCT CRACR2B MUC5AC LOC171391 POLR2L MIR210 HRAS PDDC1 PNPLA2 PTDSS2 SNORA52 MUC5B TSPAN4 CD151 CEND1 SLC25A22 DRD4 LRRC56 TOLLIP
nsv1039558 Chr.11:534242 - 672091 on Build GRCh38 Gain LOC143666 RASSF7 SCT DEAF1 MIR210HG MIR210 HRAS IRF7 CDHR5 DRD4 LMNTD2 LRRC56 PHRF1
dgv182e199 Chr.11:349830 - 943372 on Build GRCh38 Deletion LOC143666 TMEM80 TALDO1 DEAF1 MIR210HG CHID1 AP2A2 EPS8L2 IRF7 RNH1 RPLP2 CDHR5 SIGIRR LMNTD2 PHRF1 PANO1 ANO9 RASSF7 PIDD1 LOC101059906 SCT CRACR2B B4GALNT4 LOC171391 POLR2L MIR210 HRAS PDDC1 PNPLA2 PTDSS2 SNORA52 TSPAN4 CD151 CEND1 SLC25A22 DRD4 PKP3 LRRC56
nsv1053964 Chr.11:491334 - 692433 on Build GRCh38 Gain LOC143666 RASSF7 LOC101059906 SCT DEAF1 MIR210HG MIR210 HRAS IRF7 RNH1 PTDSS2 CDHR5 DRD4 LMNTD2 LRRC56 PHRF1
nsv1159791 Chr.11:461793 - 909492 on Build GRCh38 Deletion LOC143666 TMEM80 TALDO1 DEAF1 MIR210HG CHID1 EPS8L2 IRF7 RNH1 RPLP2 CDHR5 LMNTD2 PHRF1 PANO1 RASSF7 PIDD1 LOC101059906 SCT CRACR2B LOC171391 POLR2L MIR210 HRAS PDDC1 PNPLA2 PTDSS2 SNORA52 TSPAN4 CD151 CEND1 SLC25A22 DRD4 LRRC56
nsv469924 Chr.11:549119 - 609887 on Build GRCh38 Gain LOC143666 RASSF7 MIR210HG MIR210 LMNTD2 LRRC56 PHRF1

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

Gene Ontology Categories:

Function(s)


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