Human Gene UCP2 (ENST00000663595.2_7) from GENCODE V47lift37
  Description: uncoupling protein 2, transcript variant 2 (from RefSeq NM_003355.3)
Gencode Transcript: ENST00000663595.2_7
Gencode Gene: ENSG00000175567.12_18
Transcript (Including UTRs)
   Position: hg19 chr11:73,685,717-73,693,888 Size: 8,172 Total Exon Count: 8 Strand: -
Coding Region
   Position: hg19 chr11:73,686,052-73,689,423 Size: 3,372 Coding Exon Count: 6 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesGeneReviewsModel InformationMethods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr11:73,685,717-73,693,888)mRNA (may differ from genome)Protein (309 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
HGNCMalacardsMGIOMIMPubMedReactome
UniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: UCP2_HUMAN
DESCRIPTION: RecName: Full=Mitochondrial uncoupling protein 2; Short=UCP 2; AltName: Full=Solute carrier family 25 member 8; AltName: Full=UCPH;
FUNCTION: UCP are mitochondrial transporter proteins that create proton leaks across the inner mitochondrial membrane, thus uncoupling oxidative phosphorylation from ATP synthesis. As a result, energy is dissipated in the form of heat.
SUBUNIT: Acts as a dimer forming a proton channel (By similarity).
SUBCELLULAR LOCATION: Mitochondrion inner membrane; Multi-pass membrane protein.
TISSUE SPECIFICITY: Widely expressed in adult human tissues, including tissues rich in macrophages. Most expressed in white adipose tissue and skeletal muscle.
POLYMORPHISM: Genetic variations in UCP2 define the body mass index quantitative trait locus 4 (BMIQ4) [MIM:607447]. A common polymorphism in the promoter of UCP2 has been shown to be associated with a decreased risk of obesity in middle-aged individuals.
SIMILARITY: Belongs to the mitochondrial carrier family.
SIMILARITY: Contains 3 Solcar repeats.
WEB RESOURCE: Name=NIEHS-SNPs; URL="http://egp.gs.washington.edu/data/ucp2/";

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: UCP2
Diseases sorted by gene-association score: obesity bmiq4* (575), hyperinsulinism due to ucp2 deficiency* (350), familial hyperinsulinsism* (58), hyperinsulinemic hypoglycemia, familial, 2* (50), obesity (10), acute insulin response (8), neovascular glaucoma (7), hyperinsulinism (7), diabetes mellitus, noninsulin-dependent (2), overnutrition (2)
* = Manually curated disease association

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -120.40379-0.318 Picture PostScript Text
3' UTR -56.25335-0.168 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR002030 - Mit_uncoupling
IPR018108 - Mitochondrial_sb/sol_carrier
IPR023395 - Mt_carrier_dom

Pfam Domains:
PF00153 - Mitochondrial carrier protein

SCOP Domains:
103506 - Mitochondrial carrier

ModBase Predicted Comparative 3D Structure on P55851
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
 RGDEnsembl   
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0005515 protein binding
GO:0017077 oxidative phosphorylation uncoupler activity

Biological Process:
GO:0000303 response to superoxide
GO:0001666 response to hypoxia
GO:0006839 mitochondrial transport
GO:0007565 female pregnancy
GO:0007568 aging
GO:0009409 response to cold
GO:0009749 response to glucose
GO:0010942 positive regulation of cell death
GO:0032869 cellular response to insulin stimulus
GO:0032870 cellular response to hormone stimulus
GO:0034198 cellular response to amino acid starvation
GO:0043066 negative regulation of apoptotic process
GO:0051881 regulation of mitochondrial membrane potential
GO:0061179 negative regulation of insulin secretion involved in cellular response to glucose stimulus
GO:0070542 response to fatty acid
GO:0071333 cellular response to glucose stimulus
GO:0097421 liver regeneration
GO:1902600 hydrogen ion transmembrane transport
GO:1990542 mitochondrial transmembrane transport
GO:1990845 adaptive thermogenesis

Cellular Component:
GO:0005737 cytoplasm
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0031966 mitochondrial membrane


-  Descriptions from all associated GenBank mRNAs
  LF207790 - JP 2014500723-A/15293: Polycomb-Associated Non-Coding RNAs.
AK025742 - Homo sapiens cDNA: FLJ22089 fis, clone HEP16080, highly similar to HSU94592 Human uncoupling protein homolog (UCPH) mRNA.
U94592 - Homo sapiens uncoupling protein homolog (UCPH) mRNA, complete cds.
BC011737 - Homo sapiens uncoupling protein 2 (mitochondrial, proton carrier), mRNA (cDNA clone MGC:19567 IMAGE:4335185), complete cds.
JD381872 - Sequence 362896 from Patent EP1572962.
AK222557 - Homo sapiens mRNA for uncoupling protein 2 variant, clone: adSU01813.
AK222540 - Homo sapiens mRNA for uncoupling protein 2 variant, clone: adSE01386.
LF369211 - JP 2014500723-A/176714: Polycomb-Associated Non-Coding RNAs.
JD297628 - Sequence 278652 from Patent EP1572962.
JD164746 - Sequence 145770 from Patent EP1572962.
JD153927 - Sequence 134951 from Patent EP1572962.
LF369210 - JP 2014500723-A/176713: Polycomb-Associated Non-Coding RNAs.
U82819 - Homo sapiens UCP2 mRNA, complete cds.
JD258722 - Sequence 239746 from Patent EP1572962.
JD424076 - Sequence 405100 from Patent EP1572962.
JD477140 - Sequence 458164 from Patent EP1572962.
JD402792 - Sequence 383816 from Patent EP1572962.
JD341639 - Sequence 322663 from Patent EP1572962.
JD326541 - Sequence 307565 from Patent EP1572962.
CU680034 - Synthetic construct Homo sapiens gateway clone IMAGE:100020684 5' read UCP2 mRNA.
U76367 - Human uncoupling protein-2 (UCP2) mRNA, nuclear gene encoding mitochondrial protein, complete cds.
KJ892353 - Synthetic construct Homo sapiens clone ccsbBroadEn_01747 UCP2 gene, encodes complete protein.
KR710420 - Synthetic construct Homo sapiens clone CCSBHm_00012303 UCP2 (UCP2) mRNA, encodes complete protein.
KR710421 - Synthetic construct Homo sapiens clone CCSBHm_00012304 UCP2 (UCP2) mRNA, encodes complete protein.
KR710422 - Synthetic construct Homo sapiens clone CCSBHm_00012305 UCP2 (UCP2) mRNA, encodes complete protein.
KR710423 - Synthetic construct Homo sapiens clone CCSBHm_00012307 UCP2 (UCP2) mRNA, encodes complete protein.
DQ893298 - Synthetic construct clone IMAGE:100005928; FLH199500.01X; RZPDo839E0882D uncoupling protein 2 (mitochondrial, proton carrier) (UCP2) gene, encodes complete protein.
DQ896736 - Synthetic construct Homo sapiens clone IMAGE:100011196; FLH199406.01L; RZPDo839E0881D uncoupling protein 2 (mitochondrial, proton carrier) (UCP2) gene, encodes complete protein.
AB590212 - Synthetic construct DNA, clone: pFN21AE1315, Homo sapiens UCP2 gene for uncoupling protein 2, without stop codon, in Flexi system.
LF369209 - JP 2014500723-A/176712: Polycomb-Associated Non-Coding RNAs.
LF369207 - JP 2014500723-A/176710: Polycomb-Associated Non-Coding RNAs.
JD290026 - Sequence 271050 from Patent EP1572962.
JD228386 - Sequence 209410 from Patent EP1572962.
JD161811 - Sequence 142835 from Patent EP1572962.
JD391149 - Sequence 372173 from Patent EP1572962.
JD268211 - Sequence 249235 from Patent EP1572962.
JD394816 - Sequence 375840 from Patent EP1572962.
JD472028 - Sequence 453052 from Patent EP1572962.
JD349075 - Sequence 330099 from Patent EP1572962.
JD209691 - Sequence 190715 from Patent EP1572962.
JD396947 - Sequence 377971 from Patent EP1572962.
MA604788 - JP 2018138019-A/176714: Polycomb-Associated Non-Coding RNAs.
MA604787 - JP 2018138019-A/176713: Polycomb-Associated Non-Coding RNAs.
MA604786 - JP 2018138019-A/176712: Polycomb-Associated Non-Coding RNAs.
MA604784 - JP 2018138019-A/176710: Polycomb-Associated Non-Coding RNAs.
MA443367 - JP 2018138019-A/15293: Polycomb-Associated Non-Coding RNAs.

-  Biochemical and Signaling Pathways
  Reactome (by CSHL, EBI, and GO)

Protein P55851 (Reactome details) participates in the following event(s):

R-HSA-166220 FA anion diffuses laterally to UCP
R-HSA-166387 The FA anion diffuses away laterally from UCP
R-HSA-166214 FA anion flip-flops to the opposite surface
R-HSA-170026 Protons are translocated from the intermembrane space to the matrix
R-HSA-167826 The fatty acid cycling model
R-HSA-166187 Mitochondrial Uncoupling Proteins
R-HSA-167827 The proton buffering model
R-HSA-163200 Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.
R-HSA-1428517 The citric acid (TCA) cycle and respiratory electron transport
R-HSA-1430728 Metabolism

-  Other Names for This Gene
  Alternate Gene Symbols: ENST00000663595.1, NM_003355, P55851, Q4PJH8, Q53HM3, SLC25A8 , uc329kln.1, uc329kln.2, UCP2_HUMAN
UCSC ID: ENST00000663595.2_7
RefSeq Accession: NM_003355.3
Protein: P55851 (aka UCP2_HUMAN)

-  GeneReviews for This Gene
  GeneReviews article(s) related to gene UCP2:
hi (Nonsyndromic Genetic Hyperinsulinism Overview)

-  Gene Model Information
  Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.