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 MIR5691 CNV Assays ›
Gene Symbol
MIR5691
Assay Reference Genome
Location

Chr.11:9090313 on build GRCh38
Cytoband
11p15.4
Assay ID Hs03779026_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 100847015

Gene Name:

 microRNA 5691

Gene Aliases:

 -

Location:

 Chr.11:9090312-9090379 on Build GRCh38

Assay Gene Location:

 Overlaps - Exon 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
MIR5691 NR_049874.1

Target Gene Details

Entrez Gene ID:

 57758

Gene Name:

 signal peptide, CUB domain and EGF like domain containing 2

Gene Aliases:

 CEGB1, CEGF1, CEGP1

Location:

 Chr.11:9019500-9091603 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SCUBE2 NM_001170690.1 NP_001164161.1
NM_020974.2 NP_066025.2
XM_005253032.4 XP_005253089.2
XM_005253033.4 XP_005253090.2
XM_005253034.4 XP_005253091.2
XM_005253035.4 XP_005253092.2
XM_005253036.4 XP_005253093.2
XM_005253037.4 XP_005253094.2
XM_011520246.2 XP_011518548.1
XM_011520247.2 XP_011518549.1
XM_011520248.2 XP_011518550.1
XM_017018080.1 XP_016873569.1
XM_017018081.1 XP_016873570.1
XM_017018082.1 XP_016873571.1
AK123039.1 BAC85521.1
AK131552.1 BAD18686.1
BC111690.1 AAI11691.1
DN995815.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv467706 Chr.11:9056105 - 9093452 on Build GRCh38 Loss MIR5691 SCUBE2
nsv553454 Chr.11:9037645 - 9103754 on Build GRCh38 Loss MIR5691 KRT8P41 SCUBE2
nsv951307 Chr.11:9087954 - 9098353 on Build GRCh38 Deletion MIR5691 KRT8P41 SCUBE2
esv33264 Chr.11:8986065 - 9289584 on Build GRCh38 Loss NRIP3 DENND5A MIR5691 TMEM41B KRT8P41 SCUBE2

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs112511786,rs73412019] 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:

Gene Ontology Categories:

Process(es)


Back To Top

Related Products