View UCP3 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol UCP3
Gene name uncoupling protein 3 (mitochondrial, proton carrier)
Chromosome 11
Chromosomal band q13.4
Imprinted Unknown
Genomic reference NC_000011.9
Transcript reference NM_003356.3, NM_022803.2
Associated with diseases 601665
Citation reference(s) -
Curators (0) -
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants 0
Notes MSeqDR-LSDB
Date created November 12, 2013

Links to other resources
HGNC 12519
Entrez Gene 7352
PubMed articles UCP3
OMIM - Gene 602044
OMIM - Diseases 601665 (Obesity, autosomal dominant, 601665 (3))
HGMD UCP3
GeneCards UCP3
GeneTests UCP3


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001267 11 transcript variant long NM_003356.3 NP_003347.1 0
00001268 11 transcript variant short NM_022803.2 NP_073714.1 0


Copyright & disclaimer
; NuclearMitome http://www.transgenomic.com ; MitoPhenome http://mitophenome.org ; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium