UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:None
HGNC Symbol:SLC22A23
HGNC Description:solute carrier family 22, member 23
HGNC ID:21106
Superfamily:SLC
Chromosome:Chr.6(-): 3269207-3456954 GRCh37
Location:6p25.2
OMIM:611697
OMIM Phenotype:None
Accessions:None
Nucleotide RefSeq:NM_015482
Protein RefSeq:NP_056297
Entrez:63027
Ensembl:ENSG00000137266
Isoforms:4
Evidence:None
Tissues:None
Type:protein-coding
Sets:None
PharmGKB ID:
HPRD ID:12904
Substrates:None
Trivial Names:C6orf85
Transcripts:NM_015482.1 [Chr.6(-): 3269207-3456793 GRCh37]
NM_021945.5 [Chr.6(-): 3269207-3445218 GRCh37]
XM_005249285.1 [Chr.6(-): 3269207-3456954 GRCh37]
XM_005249286.1 [Chr.6(-): 3269207-3445247 GRCh37]
ENST00000380298 [Chr.6(-): 3323576-3456793 GRCh37]
ENST00000380302 [Chr.6(-): 3272008-3445247 GRCh37]
ENST00000406686 [Chr.6(-): 3269692-3456793 GRCh37]
ENST00000433689 [Chr.6(-): 3323576-3324399 GRCh37]
ENST00000436008 [Chr.6(-): 3269196-3457256 GRCh37]
ENST00000467144 [Chr.6(-): 3287218-3324417 GRCh37]
ENST00000467177 [Chr.6(-): 3284108-3439652 GRCh37]
ENST00000482874 [Chr.6(-): 3273590-3284354 GRCh37]
ENST00000485307 [Chr.6(-): 3283699-3456277 GRCh37]
ENST00000490273 [Chr.6(-): 3273064-3445218 GRCh37]
ENST00000496753 [Chr.6(-): 3290000-3378220 GRCh37]
ENST00000497691 [Chr.6(-): 3272008-3445203 GRCh37]
Annotation History:View Events (19)

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 SLC22A23.

Variant Data

View all PMT variants for SLC22A23 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:

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.