Gene: MCU (mitochondrial calcium uniporter)  Homo sapiens
Symbol: MCU
Name: mitochondrial calcium uniporter
Description: This gene encodes a calcium transporter that localizes to the mitochondrial inner membrane. The encoded protein interacts with mitochondrial calcium uptake 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: C10orf42; calcium uniporter protein, mitochondrial; CCDC109A; coiled-coil domain containing 109A; coiled-coil domain-containing protein 109A; FLJ46135; OTTHUMP00000019789; OTTHUMP00000019790
Orthologs: Mus musculus : Mcu (mitochondrial calcium uniporter)  MGI
Rattus norvegicus : Mcu (mitochondrial calcium uniporter)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_11074,825,250 - 75,020,129+NCBI
Human Genome Assembly HuRef1068,445,749 - 68,641,292+NCBI
Human Genome Assembly GRCh371074,451,889 - 74,647,452+NCBI
Human Celera Assembly1067,737,028 - 67,932,591+NCBI
Human Genome Assembly Build 361074,121,895 - 74,317,458+NCBI
Human Cytogenetic Map10q22.1 NCBI
Human Genome Assembly1074,121,894 - 74,317,456 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)

Annotation    (Toggle Detail/Summary View)

Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
  
More on MCU
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 1343502
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2013-03-06
Status: ACTIVE



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