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See other ST5 CNV Assays ›
Gene Symbol
ST5
Assay Reference Genome
Location

Chr.11:8710213 on build GRCh38
Cytoband
11p15.4
Assay ID Hs06271055_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 6764

Gene Name:

 suppression of tumorigenicity 5

Gene Aliases:

 DENND2B, HTS1, p126

Location:

 Chr.11:8693352-8910951 on Build GRCh38

Assay Gene Location:

 Within Intron 25
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
ST5 NM_005418.3 NP_005409.3
NM_139157.2 NP_631896.1
NM_213618.1 NP_998783.1
XM_005253077.1 XP_005253134.1
XM_005253083.2 XP_005253140.1
XM_011520309.1 XP_011518611.1
XM_011520310.1 XP_011518612.1
XM_011520311.2 XP_011518613.1
XM_011520312.1 XP_011518614.1
XM_011520313.1 XP_011518615.1
XM_011520314.1 XP_011518616.1
XM_011520315.1 XP_011518617.1
XM_011520316.1 XP_011518618.1
XM_011520317.1 XP_011518619.1
XM_011520318.1 XP_011518620.1
XM_011520319.2 XP_011518621.1
XM_011520320.1 XP_011518622.1
XM_011520321.2 XP_011518623.1
XM_011520322.1 XP_011518624.1
XM_011520323.2 XP_011518625.2
XM_011520324.2 XP_011518626.2
XM_011520325.1 XP_011518627.1
XM_011520326.1 XP_011518628.1
XM_011520327.1 XP_011518629.1
XM_011520328.1 XP_011518630.1
XM_011520329.1 XP_011518631.1
XM_017018182.1 XP_016873671.1
XM_017018183.1 XP_016873672.1
XM_017018184.1 XP_016873673.1
XM_017018185.1 XP_016873674.1
XM_017018186.1 XP_016873675.1
XM_017018187.1 XP_016873676.1
AK126554.1 BAC86590.1
AK127763.1
AK293245.1
AK302824.1
AK309929.1
AK312305.1
AK312758.1
BC036655.1 AAH36655.1
BX647431.1
S45936.1 AAB23647.1
U15131.1 AAC50925.1
U15779.1 AAB97097.1
U15780.1 AAC50926.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv951306 Chr.11:8701054 - 8735653 on Build GRCh38 Deletion ST5

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More Information


Additional Information:

For this assay, SNP(s) [rs117396370] 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

Gene Ontology Categories:

Function(s) Process(es)


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