UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:GLUT9
HGNC Symbol:SLC2A9
HGNC Description:solute carrier family 2 (facilitated glucose transporter), member 9
HGNC ID:13446
Chromosome:Chr.4(-): 9827848-10041872 GRCh37
OMIM Phenotype:None
Nucleotide RefSeq:NM_001001290
Protein RefSeq:NP_001001290
PharmGKB ID:PA37771
HPRD ID:05848
Trivial Names:GLUT9, GLUTX, UAQTL2, URATv1
Transcripts:NM_001001290.1 [Chr.4(-): 9827848-10041872 GRCh37]
NM_020041.2 [Chr.4(-): 9827848-10023114 GRCh37]
XM_005248176.1 [Chr.4(-): 9880643-10041834 GRCh37]
ENST00000264784 [Chr.4(-): 9827848-10023107 GRCh37]
ENST00000309065 [Chr.4(-): 9827850-10041872 GRCh37]
ENST00000481042 [Chr.4(-): 10035849-10042012 GRCh37]
ENST00000503280 [Chr.4(-): 9800702-9909969 GRCh37]
ENST00000503803 [Chr.4(-): 9781431-9889266 GRCh37]
ENST00000505104 [Chr.4(-): 9881830-10041834 GRCh37]
ENST00000505506 [Chr.4(-): 9997293-10020699 GRCh37]
ENST00000506583 [Chr.4(-): 9827848-10056499 GRCh37]
ENST00000506839 [Chr.4(-): 9987292-10020918 GRCh37]
ENST00000508585 [Chr.4(-): 9772777-9828224 GRCh37]
ENST00000509214 [Chr.4(-): 10027348-10030924 GRCh37]
ENST00000512342 [Chr.4(-): 9800284-9889266 GRCh37]
ENST00000513129 [Chr.4(-): 9982216-10056560 GRCh37]

GTEx Expression by Gene and Transcript

The heat map summarizes relative expression by tissue type at two levels of tissue detail, e.g., 'Brain' and 'Brain - Amygdala'. Choose among four calculated expression values, including mean and median RPKM values, and quantile normalized (QN) distributions of these values. (Note that differences between some distributions are subtle.) The coloring is relative to the mean of all displayed values. All values are log base 2. (See also PMT GTEx Expression Plotting.) Click on a transcript or tissue to resort the data.

Expression values:
No expression data exists for SLC2A9.

Variant Data

View all PMT variants for SLC2A9 on UCSC Genome Browser
Showing SNP features for transcript:   
1000 Genomes  

20141104 phase 3 variant call set of the 20130502 sequence freeze and alignments for SNPs and short indels (indels > 255 and structural variants are not included here). This variant set contains 2504 individuals from 26 populations (mouse over population column heading for population sizes).
Showing gene variants in regions defined by NCBI RefSeq exons, putative promoter, and PMT resequencing assays.
Note: Frequencies are calculated directly from reported genotypes and may vary from consensus frequencies reported by the 1000 Genomes project, which relied on additional data and the GATK tool Variant Quality Score Recalibrator.
dbSNP build 142.
Array availability: I - found on Illumina Human1M-Duo BeadChip (2011-04-21)  A - found on Affymetrix Genome-Wide SNP Array 6.0 (2011-06-21)  
Download the SNP table data as a tab-delimited file.

Transmembrane prediction: TOPO2 image is not available.