UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:UCP4
HGNC Symbol:SLC25A27
HGNC Description:solute carrier family 25, member 27
HGNC ID:21065
Chromosome:Chr.6(+): 46620652-46645927 GRCh37
OMIM Phenotype:None
Nucleotide RefSeq:NM_004277
Protein RefSeq:NP_004268
PharmGKB ID:PA134970102
HPRD ID:15358
Trivial Names:UCP4, RP11-446F17.2
Transcripts:NM_004277.4 [Chr.6(+): 46620652-46645927 GRCh37]
NM_001204051.1 [Chr.6(+): 46620652-46645927 GRCh37]
NM_001204052.1 [Chr.6(+): 46620652-46645927 GRCh37]
XM_005249485.1 [Chr.6(+): 46620682-46645927 GRCh37]
XM_005249483.1 [Chr.6(+): 46620682-46644377 GRCh37]
XM_005249484.1 [Chr.6(+): 46621080-46645927 GRCh37]
ENST00000371347 [Chr.6(+): 46620678-46645930 GRCh37]
ENST00000411689 [Chr.6(+): 46620679-46644750 GRCh37]
ENST00000452689 [Chr.6(+): 46620722-46644513 GRCh37]
ENST00000603486 [Chr.6(+): 46626400-46636484 GRCh37]
ENST00000603501 [Chr.6(+): 46644250-46645471 GRCh37]
ENST00000604127 [Chr.6(+): 46630197-46645654 GRCh37]
ENST00000604217 [Chr.6(+): 46630197-46638965 GRCh37]
ENST00000604616 [Chr.6(+): 46632612-46644740 GRCh37]
ENST00000604908 [Chr.6(+): 46626490-46637945 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 SLC25A27.

Variant Data

View all PMT variants for SLC25A27 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.