UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:UCP2
HGNC Symbol:UCP2
HGNC Description:uncoupling protein 2 (mitochondrial, proton carrier)
HGNC ID:12518
Superfamily:SLC
Chromosome:Chr.11(-): 73685716-73693889 GRCh37
Location:11q13
OMIM:601693
OMIM Phenotype:Obesity, susceptibility to
Accessions:AF096289
Nucleotide RefSeq:NM_003355
Protein RefSeq:NP_003346
Entrez:7351
Ensembl:ENSG00000175567
Isoforms:1
Evidence:None
Tissues:None
Type:protein-coding
Sets:0
PharmGKB ID:
HPRD ID:03410
Substrates:None
Trivial Names:UCPH, BMIQ4, SLC25A8
Transcripts:NM_003355.2 [Chr.11(-): 73685716-73693889 GRCh37]
ENST00000310473 [Chr.11(-): 73685712-73694352 GRCh37]
ENST00000536983 [Chr.11(-): 73685754-73693875 GRCh37]
ENST00000539330 [Chr.11(-): 73692193-73693888 GRCh37]
ENST00000539764 [Chr.11(-): 73689326-73691983 GRCh37]
ENST00000541027 [Chr.11(-): 73689741-73693888 GRCh37]
ENST00000542615 [Chr.11(-): 73689622-73693888 GRCh37]
ENST00000543714 [Chr.11(-): 73689236-73693888 GRCh37]
ENST00000544615 [Chr.11(-): 73685897-73689186 GRCh37]
ENST00000545212 [Chr.11(-): 73686575-73688051 GRCh37]
ENST00000545562 [Chr.11(-): 73687686-73688109 GRCh37]
Annotation History:View Events (1)

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 UCP2.

Variant Data

View all PMT variants for UCP2 on UCSC Genome Browser
Showing SNP features for transcript: NM_003355  
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.