UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:None
HGNC Symbol:SLC25A36
HGNC Description:solute carrier family 25 (pyrimidine nucleotide carrier ), member 36
HGNC ID:25554
Chromosome:Chr.3(+): 140660662-140698785 GRCh37
OMIM Phenotype:None
Nucleotide RefSeq:NM_001104647
Protein RefSeq:NP_001098117
PharmGKB ID:
HPRD ID:07688
Trivial Names:PNC2
Transcripts:NM_001104647.1 [Chr.3(+): 140660662-140698785 GRCh37]
NM_018155.2 [Chr.3(+): 140660662-140698785 GRCh37]
XM_005247574.1 [Chr.3(+): 140660675-140698781 GRCh37]
XM_005247575.1 [Chr.3(+): 140686799-140698781 GRCh37]
ENST00000324194 [Chr.3(+): 140660729-140695492 GRCh37]
ENST00000393015 [Chr.3(+): 140660695-140685847 GRCh37]
ENST00000446041 [Chr.3(+): 140660672-140698775 GRCh37]
ENST00000453248 [Chr.3(+): 140660743-140695323 GRCh37]
ENST00000502594 [Chr.3(+): 140660737-140695325 GRCh37]
ENST00000502756 [Chr.3(+): 140660685-140675911 GRCh37]
ENST00000502866 [Chr.3(+): 140685622-140692831 GRCh37]
ENST00000507429 [Chr.3(+): 140660729-140685053 GRCh37]
ENST00000511757 [Chr.3(+): 140689207-140695489 GRCh37]
ENST00000512023 [Chr.3(+): 140675367-140695128 GRCh37]
ENST00000512506 [Chr.3(+): 140675469-140695124 GRCh37]
ENST00000513887 [Chr.3(+): 140661304-140689812 GRCh37]
ENST00000514629 [Chr.3(+): 140692508-140695305 GRCh37]
ENST00000515813 [Chr.3(+): 140660710-140682313 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 SLC25A36.

Variant Data

View all PMT variants for SLC25A36 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.