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 ISLR CNV Assays ›
Gene Symbol
ISLR
Assay Reference Genome
Location

Chr.15:74176474 on build GRCh38
Cytoband
15q24.1
Assay ID Hs00518797_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 3671

Gene Name:

 immunoglobulin superfamily containing leucine rich repeat

Gene Aliases:

 HsT17563, Meflin

Location:

 Chr.15:74173746-74176871 on Build GRCh38

Assay Gene Location:

 Within Exon 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ISLR NM_005545.3 2 1898 NP_005536.1
NM_201526.1 2 1714 NP_958934.1
AB003184.1 2 1714 BAA22848.1
AB024536.1 2 1898 BAA85970.1
AK000817.1 2 1898
AK074668.1 2 2306
AK223267.1 2 1730 BAD96987.1
AK225606.1 3 1350
AY358871.1 2 1974 AAQ89230.1
BC022478.1 2 1703 AAH22478.1
BC111013.1 2 1808 AAI11014.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv833053 Chr.15:74067815 - 74262799 on Build GRCh38 Loss LOC732265 ISLR GOLGA6A STRA6 ISLR2 CCDC33 LOC283731
nsv1050884 Chr.15:74102642 - 74197072 on Build GRCh38 Gain ISLR STRA6 ISLR2 LOC283731
nsv833054 Chr.15:74165302 - 74332942 on Build GRCh38 Loss ISLR STRA6 CCDC33
nsv1121512 Chr.15:72670085 - 75273877 on Build GRCh38 Deletion NEO1 PML C15orf39 EDC3 MIR4513 LOC283731 GOLGA6C MIR6881 BBS4 CYP1A2 TBC1D21 LOC102723750 LMAN1L NPTN ADPGK-AS1 PPCDC LOC732265 MPI LOC107984728 ULK3 HIGD2B LOC101929333 NPTN-IT1 SEMA7A ISLR2 LOXL1 C15orf59-AS1 HCN4 LOXL1-AS1 C15orf59 ARID3B SCAMP5 COX5A REC114 UBL7 UBL7-AS1 GOLGA6A STRA6 CPLX3 LOC105376731 ADPGK RPP25 CYP1A1 FAM219B CD276 LOC729739 CCDC33 MIR6882 STOML1 ISLR SCAMP2 CSK CYP11A1 CLK3

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs114902568] 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:

Gene Ontology Categories:

Function(s)


Back To Top

Related Products