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

Chr.7:33922164 on build GRCh38
Cytoband
7p14.3
Assay ID Hs05019943_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 168667

Gene Name:

 BMP binding endothelial regulator

Gene Aliases:

 CRIM3, CV-2, CV2

Location:

 Chr.7:33904911-34155872 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
BMPER NM_133468.4 NP_597725.1
XM_005249633.2 XP_005249690.1
XM_017011800.1 XP_016867289.1
XM_017011801.1 XP_016867290.1
AK289963.1
AY324650.1 AAP89012.1
BC060868.1 AAH60868.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
dgv1080e201 Chr.7:32621750 - 35008557 on Build GRCh38 Deletion RP9 RP9P ZNRF2P1 DPY19L1 NPSR1 BBS9 DPY19L1P1 FKBP9 LOC100421336 BMPER MIR550A2 KBTBD2 MIR550B2 MIR548N LINC00997 NT5C3A DPY19L1P2 NPSR1-AS1 FLJ20712
esv3612778 Chr.7:33861781 - 33942872 on Build GRCh38 Loss BMPER
esv3891097 Chr.7:33915559 - 34483233 on Build GRCh38 Gain BMPER NPSR1-AS1
esv3612772 Chr.7:33730657 - 34432276 on Build GRCh38 Loss BMPER NPSR1-AS1
nsv1024493 Chr.7:33733357 - 34425137 on Build GRCh38 Loss BMPER NPSR1-AS1
nsv1135982 Chr.7:32794601 - 34893593 on Build GRCh38 Deletion BMPER RP9 RP9P KBTBD2 NPSR1 NT5C3A BBS9 DPY19L1P2 NPSR1-AS1 FKBP9 FLJ20712 LOC100421336
nsv436907 Chr.7:32668474 - 34999437 on Build GRCh38 Insertion RP9 RP9P ZNRF2P1 DPY19L1 NPSR1 BBS9 DPY19L1P1 FKBP9 LOC100421336 BMPER MIR550A2 KBTBD2 MIR550B2 MIR548N LINC00997 NT5C3A DPY19L1P2 NPSR1-AS1 FLJ20712

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More Information


Additional Information:

For this assay, SNP(s) [rs73310818] 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 Intronic Non-exonic DGV Variation

Panther Classification:

Molecular Function -

extracellular matrix protein

Gene Ontology Categories:

Function(s)


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