UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:FLJ00171
HGNC Symbol:SLC37A2
HGNC Description:solute carrier family 37 (glucose-6-phosphate transporter), member 2
HGNC ID:20644
Superfamily:SLC
Chromosome:Chr.11(+): 124932963-124960412 GRCh37
Location:11q24.2
OMIM:
OMIM Phenotype:None
Accessions:BC051314
Nucleotide RefSeq:NM_198277
Protein RefSeq:NP_938018
Entrez:219855
Ensembl:ENSG00000134955
Isoforms:2
Evidence:None
Tissues:bone marrow and faintly in spleen
Type:protein-coding
Sets:0
PharmGKB ID:PA134917577
HPRD ID:15380
Substrates:None
Trivial Names:pp11662
Transcripts:NM_198277.2 [Chr.11(+): 124933013-124960412 GRCh37]
NM_001145290.1 [Chr.11(+): 124933013-124960412 GRCh37]
ENST00000298280 [Chr.11(+): 124933013-124959131 GRCh37]
ENST00000308074 [Chr.11(+): 124933232-124959131 GRCh37]
ENST00000403796 [Chr.11(+): 124932963-124959131 GRCh37]
ENST00000407458 [Chr.11(+): 124933013-124956127 GRCh37]
ENST00000525837 [Chr.11(+): 124953035-124956293 GRCh37]
ENST00000526405 [Chr.11(+): 124933231-124959131 GRCh37]
ENST00000532000 [Chr.11(+): 124933198-124950543 GRCh37]
Annotation History:View Events (3)

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.

Tissues:
Expression values:
No expression data exists for SLC37A2.

Variant Data

View all PMT variants for SLC37A2 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.