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 SLC34A1 CNV Assays ›
Gene Symbol
SLC34A1
Assay Reference Genome
Location

Chr.5:177385201 on build GRCh38
Cytoband
5q35.3
Assay ID Hs03544094_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 6569

Gene Name:

 solute carrier family 34 member 1

Gene Aliases:

 FRTS2, HCINF2, NAPI-3, NPHLOP1, NPT2, NPTIIa, SLC11, SLC17A2

Location:

 Chr.5:177384431-177412021 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SLC34A1 NM_001167579.1 NP_001161051.1
NM_003052.4 NP_003043.3
AK096088.1 BAC04699.1
AK298299.1
BC035294.1
BC050385.1 AAH50385.1
BC053349.1 AAH53349.1
BP275443.1
L13258.1 AAA36354.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv471057 Chr.5:177310308 - 177469411 on Build GRCh38 Loss PFN3 DBN1 LMAN2 SLC34A1 MXD3 GRK6 PRR7 F12 RGS14 PRR7-AS1
nsv509103 Chr.5:177308751 - 177414575 on Build GRCh38 Insertion PFN3 LMAN2 SLC34A1 MXD3 F12 RGS14
nsv600364 Chr.5:177299634 - 177432847 on Build GRCh38 Loss PRELID1 NSD1 PFN3 LMAN2 SLC34A1 MXD3 GRK6 F12 RAB24 RGS14
dgv10184n54 Chr.5:177357511 - 177469411 on Build GRCh38 Loss PFN3 DBN1 SLC34A1 GRK6 PRR7 F12 RGS14 PRR7-AS1
nsv1161313 Chr.5:177356552 - 177463415 on Build GRCh38 Duplication PFN3 DBN1 SLC34A1 GRK6 PRR7 F12 RGS14 PRR7-AS1
nsv1161312 Chr.5:177322159 - 177405557 on Build GRCh38 Deletion PFN3 LMAN2 SLC34A1 F12 RGS14
nsv1161311 Chr.5:177305104 - 177546474 on Build GRCh38 Duplication PRELID1 PFN3 FAM193B LMAN2 MXD3 F12 RGS14 DOK3 DBN1 SLC34A1 GRK6 PRR7 DDX41 PDLIM7 PRR7-AS1

Back To Top

More Information


Additional Information:

For this assay, SNP(s) [rs79117479] 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 -

secondary carrier transporter

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products