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 ITGB7 CNV Assays ›
Gene Symbol
ITGB7
Assay Reference Genome
Location

Chr.12:53191421 on build GRCh38
Cytoband
12q13.13
Assay ID Hs00144819_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 3695

Gene Name:

 integrin subunit beta 7

Gene Aliases:

 -

Location:

 Chr.12:53191318-53207376 on Build GRCh38

Assay Gene Location:

 Within Exon 16
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ITGB7 NM_000889.2 16 2764 NP_000880.1
NR_104181.1 12 2003
XM_005268851.3 16 2721 XP_005268908.1
XM_005268852.4 15 2637 XP_005268909.1
XM_006719376.3 16 2928 XP_006719439.1
AI804573.1 1 115
AK298239.1 15 2298
BC015916.1 15 2603 AAH15916.1
M62880.1 15 2645 AAA59185.1
M68892.1 15 2683 AAA59184.1
S80335.1 15 2683 AAB21332.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv832417 Chr.12:53075874 - 53254231 on Build GRCh38 Gain ZNF740 IGFBP6 SOAT2 MFSD5 CSAD SPRYD3 RARG ITGB7
nsv558994 Chr.12:53103618 - 53277765 on Build GRCh38 Loss ZNF740 SOAT2 ESPL1 MFSD5 CSAD RARG ITGB7
dgv2645n54 Chr.12:53099603 - 53227927 on Build GRCh38 Loss ZNF740 IGFBP6 SOAT2 CSAD RARG ITGB7
nsv517066 Chr.12:53006394 - 53340722 on Build GRCh38 Loss MIR6757 C12orf10 AAAS SP7 SOAT2 ESPL1 MFSD5 CSAD RARG ITGB7 ZNF740 IGFBP6 LOC283335 EIF4B PFDN5 TNS2 SPRYD3
dgv2644n54 Chr.12:53064109 - 53211560 on Build GRCh38 Loss ZNF740 IGFBP6 TNS2 SOAT2 CSAD SPRYD3 RARG ITGB7
nsv469404 Chr.12:53124036 - 53227927 on Build GRCh38 Loss ZNF740 SOAT2 CSAD RARG ITGB7

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs80201470] 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 Exonic DGV Variation

Panther Classification:

Molecular Function -

integrin

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products