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Gene Symbol
SLC2A9
Assay Reference Genome
Location

Chr.4:9824497 on build GRCh38
Cytoband
4p16.1
Assay ID Hs04862735_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 56606

Gene Name:

 solute carrier family 2 member 9

Gene Aliases:

 GLUT9, GLUTX, UAQTL2, URATv1

Location:

 Chr.4:9771125-10040248 on Build GRCh38

Assay Gene Location:

 Within Intron 21
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SLC2A9 XM_006713968.3 XP_006714031.1
XM_011513856.2 XP_011512158.1
XM_011513857.1 XP_011512159.1
XM_011513858.1 XP_011512160.1
XM_011513859.2 XP_011512161.1
XM_011513860.2 XP_011512162.1
XM_011513861.2 XP_011512163.1
XM_011513862.2 XP_011512164.1
XM_011513863.2 XP_011512165.1
XM_011513864.2 XP_011512166.1
XM_011513867.2 XP_011512169.1
XM_017008457.1 XP_016863946.1
XM_017008458.1 XP_016863947.1
XM_017008459.1 XP_016863948.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv2759222 Chr.4:8520446 - 10274843 on Build GRCh38 Gain+Loss USP17L10 USP17L13 USP17L15 USP17L30 GPR78 USP17L21 USP17L29 OR7E85P CPZ USP17L25 USP17L22 USP17L11 USP17L19 DRD5 OR7E35P HMX1 USP17L17 MIR548I2 USP17L12 USP17L6P USP17L20 WDR1 LOC650293 USP17L18 SLC2A9 MIR3138 USP17L28 LOC101928532 DEFB131 USP17L5 USP17L27 FAM86KP LOC100133128 USP17L26 USP17L24 USP17L9P
esv3599593 Chr.4:9722281 - 9836957 on Build GRCh38 Gain SLC2A9 DRD5 OR7E35P
esv3599589 Chr.4:9651137 - 10489676 on Build GRCh38 Gain ZNF518B WDR1 SLC2A9 MIR3138 DRD5 OR7E35P
nsv1005698 Chr.4:8434559 - 10248775 on Build GRCh38 Gain USP17L10 USP17L13 USP17L15 USP17L30 GPR78 ACOX3 TRMT44 USP17L21 USP17L29 OR7E85P CPZ USP17L25 USP17L22 USP17L11 USP17L19 DRD5 OR7E35P HMX1 USP17L17 MIR548I2 USP17L12 USP17L6P USP17L20 WDR1 LOC650293 USP17L18 SLC2A9 MIR3138 USP17L28 LOC101928532 DEFB131 USP17L5 USP17L27 FAM86KP LOC100133128 USP17L26 USP17L24 USP17L9P
dgv5108n100 Chr.4:9427573 - 9828584 on Build GRCh38 Gain MIR548I2 OR7E85P DEFB131 SLC2A9 DRD5 OR7E35P
dgv5118n100 Chr.4:9800522 - 9976790 on Build GRCh38 Gain SLC2A9
dgv5119n100 Chr.4:9804044 - 9895896 on Build GRCh38 Loss SLC2A9
nsv1014335 Chr.4:9435268 - 10687720 on Build GRCh38 Gain CLNK MIR548I2 OR7E85P DEFB131 ZNF518B WDR1 SLC2A9 MIR3138 DRD5 OR7E35P
dgv5117n100 Chr.4:9711988 - 10222212 on Build GRCh38 Gain WDR1 SLC2A9 MIR3138 DRD5 OR7E35P

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More Information


Additional Information:

For this assay, SNP(s) [rs79095673] 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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