UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:SLC10A4
HGNC Symbol:SLC10A4
HGNC Description:solute carrier family 10, member 4
HGNC ID:22980
Chromosome:Chr.4(+): 48485360-48491541 GRCh37
OMIM Phenotype:None
Nucleotide RefSeq:NM_152679
Protein RefSeq:NP_689892
PharmGKB ID:PA134941471
HPRD ID:11562
Trivial Names:P4
Transcripts:NM_152679.3 [Chr.4(+): 48485360-48491541 GRCh37]
ENST00000273861 [Chr.4(+): 48485360-48491213 GRCh37]
Annotation History:View Events (2)

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 SLC10A4.

Variant Data

View all PMT variants for SLC10A4 on UCSC Genome Browser
Showing SNP features for transcript: NM_152679  
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:

Non-synonymous amino acid changes shown in red, indels (insertions and deletions) in blue, and synonymous changes in green. Exon(s) indicated by black outlines.