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 SLC26A1 CNV Assays ›
Gene Symbol
SLC26A1
Assay Reference Genome
Location

Chr.4:985099 on build GRCh38
Cytoband
4p16.3
Assay ID Hs04273325_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 10861

Gene Name:

 solute carrier family 26 member 1

Gene Aliases:

 CAON, EDM4, SAT-1, SAT1

Location:

 Chr.4:979073-993440 on Build GRCh38

Assay Gene Location:

 Within Intron 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SLC26A1 NM_134425.2 NP_602297.1
BC015517.2 AAH15517.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1003219 Chr.4:776106 - 1111676 on Build GRCh38 Gain DGKQ CPLX1 GAK LOC100129917 IDUA FGFRL1 RNF212 TMEM175 SLC26A1
nsv822428 Chr.4:968896 - 1028144 on Build GRCh38 Gain DGKQ IDUA FGFRL1 SLC26A1
nsv593226 Chr.4:948218 - 1025223 on Build GRCh38 Loss DGKQ IDUA FGFRL1 TMEM175 SLC26A1
esv3599384 Chr.4:974637 - 1010875 on Build GRCh38 Gain IDUA SLC26A1
nsv822425 Chr.4:546316 - 1420011 on Build GRCh38 Loss DGKQ PCGF3 SPON2 CRIPAK FGFRL1 UVSSA LOC101928521 MFSD7 LOC100130872 TMED11P MAEA RNF212 CTBP1 CTBP1-AS LOC101928548 CPLX1 IDUA CTBP1-AS2 TMEM175 ATP5I SLC26A1 GAK LOC100129917 LOC107986211 NKX1-1 MYL5 LOC105374344 PDE6B
nsv4196 Chr.4:961755 - 1004599 on Build GRCh38 Deletion DGKQ IDUA SLC26A1
esv3599385 Chr.4:983183 - 986434 on Build GRCh38 Loss SLC26A1
nsv469998 Chr.4:815805 - 1093743 on Build GRCh38 Loss DGKQ CPLX1 GAK IDUA FGFRL1 RNF212 TMEM175 SLC26A1
nsv1008352 Chr.4:819605 - 1041628 on Build GRCh38 Gain DGKQ CPLX1 GAK IDUA FGFRL1 TMEM175 SLC26A1
dgv1450e212 Chr.4:976838 - 986842 on Build GRCh38 Gain SLC26A1

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs192526712] 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 -

transporter

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products