UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:SUT1
HGNC Symbol:SLC13A4
HGNC Description:solute carrier family 13 (sodium/sulfate symporter), member 4
HGNC ID:15827
Superfamily:SLC
Chromosome:Chr.7(-): 135365979-135412943 GRCh37
Location:7q33
OMIM:604309
OMIM Phenotype:None
Accessions:AF169301,BC030689
Nucleotide RefSeq:NM_012450
Protein RefSeq:NP_036582
Entrez:26266
Ensembl:ENSG00000164707
Isoforms:3
Evidence:None
Tissues:None
Type:protein-coding
Sets:0
PharmGKB ID:PA38045
HPRD ID:10372
Substrates:None
Trivial Names:SUT1, SUT-1
Transcripts:NM_012450.2 [Chr.7(-): 135365985-135412933 GRCh37]
XM_005250261.1 [Chr.7(-): 135365979-135412943 GRCh37]
XM_005250262.1 [Chr.7(-): 135368078-135412943 GRCh37]
ENST00000354042 [Chr.7(-): 135365985-135412934 GRCh37]
ENST00000378428 [Chr.7(-): 135392889-135413974 GRCh37]
ENST00000422620 [Chr.7(-): 135406141-135414006 GRCh37]
ENST00000471405 [Chr.7(-): 135365989-135412952 GRCh37]
ENST00000478310 [Chr.7(-): 135392185-135412922 GRCh37]
ENST00000480376 [Chr.7(-): 135384112-135390555 GRCh37]
ENST00000491630 [Chr.7(-): 135365985-135370433 GRCh37]
Annotation History:View Events (20)

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 SLC13A4.

Variant Data

View all PMT variants for SLC13A4 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.