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 TMEM80 CNV Assays ›
Gene Symbol
TMEM80
Assay Reference Genome
Location

Chr.11:704167 on build GRCh38
Cytoband
11p15.5
Assay ID Hs02576497_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 283232

Gene Name:

 transmembrane protein 80

Gene Aliases:

 -

Location:

 Chr.11:695386-705028 on Build GRCh38

Assay Gene Location:

 Overlaps Exon 5 - Intron 5
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
TMEM80 NM_001042463.2 NP_001035928.2
NM_001276253.1 NP_001263182.1
NM_001276274.1 NP_001263203.1
NM_174940.3 NP_777600.3
XM_006718206.3 XP_006718269.3
XM_017017600.1 XP_016873089.1
AI739035.1
AK124309.1
AK302585.1
BC008671.1
CA443683.1
CB044312.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv469923 Chr.11:378188 - 1302334 on Build GRCh38 Loss SCT CHID1 MUC5B POLR2L MIR6744 PNPLA2 LOC143666 RPLP2 ANO9 MIR210 RNH1 MUC2 TSPAN4 RASSF7 PTDSS2 MIR210HG PDDC1 TOLLIP HRAS LRRC56 LOC101059906 CEND1 DEAF1 PHRF1 CDHR5 SLC25A22 TMEM80 MUC5AC LOC101927503 PKP3 SIGIRR IRF7 EPS8L2 TALDO1 LOC171391 MUC6 CRACR2B PANO1 B4GALNT4 DRD4 PIDD1 LMNTD2 AP2A2 SNORA52 CD151
nsv522733 Chr.11:702250 - 752059 on Build GRCh38 Loss TMEM80 EPS8L2 TALDO1
esv2759794 Chr.11:409846 - 1336162 on Build GRCh38 Loss SCT CHID1 MUC5B POLR2L MIR6744 PNPLA2 LOC143666 RPLP2 ANO9 MIR210 RNH1 MUC2 TSPAN4 RASSF7 PTDSS2 MIR210HG PDDC1 TOLLIP HRAS LRRC56 LOC101059906 CEND1 DEAF1 PHRF1 CDHR5 SLC25A22 TMEM80 MUC5AC LOC101927503 SIGIRR IRF7 EPS8L2 TALDO1 TOLLIP-AS1 LOC171391 MUC6 CRACR2B PANO1 DRD4 PIDD1 LMNTD2 AP2A2 SNORA52 CD151
nsv832043 Chr.11:631027 - 758602 on Build GRCh38 Loss DEAF1 TMEM80 DRD4 EPS8L2 TALDO1
nsv552869 Chr.11:702097 - 727446 on Build GRCh38 Loss TMEM80 EPS8L2
dgv182e199 Chr.11:349830 - 943372 on Build GRCh38 Deletion SCT CHID1 POLR2L PNPLA2 LOC143666 RPLP2 ANO9 MIR210 RNH1 TSPAN4 RASSF7 PTDSS2 MIR210HG PDDC1 HRAS LRRC56 LOC101059906 CEND1 DEAF1 PHRF1 CDHR5 SLC25A22 TMEM80 PKP3 SIGIRR IRF7 EPS8L2 TALDO1 LOC171391 CRACR2B PANO1 B4GALNT4 DRD4 PIDD1 LMNTD2 AP2A2 SNORA52 CD151
nsv1159791 Chr.11:461793 - 909492 on Build GRCh38 Deletion SCT CHID1 POLR2L PNPLA2 LOC143666 RPLP2 MIR210 RNH1 TSPAN4 RASSF7 PTDSS2 MIR210HG PDDC1 HRAS LRRC56 LOC101059906 CEND1 DEAF1 PHRF1 CDHR5 SLC25A22 TMEM80 IRF7 EPS8L2 TALDO1 LOC171391 CRACR2B PANO1 DRD4 PIDD1 LMNTD2 SNORA52 CD151

Back To Top

More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

Back To Top

Related Products