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Symbol MT-CO3 contributors: npt - updated : 13-03-2006
HGNC name mitochondrially encoded cytochrome c oxidase III
HGNC id 7422
Corresponding disease
LHON Leber hereditary optic neuropathy
MTCO3 mitochondrial myopathy, with recurrent myoglobinuria (COX deficiency)
Location mt      Physical location : -
Synonym name cytochrome c oxidase III
Synonym symbol(s) MTCO3, COX3
EC.number 1.9.3.1
DNA
TYPE functioning gene
MAPPING cloned N linked N status provisional
RNA
TRANSCRIPTS type messenger
EXPRESSION
Type
constitutive of
   expressed in (based on citations)
organ(s)
cell lineage
cell lines
fluid/secretion
at STAGE
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
HOMOLOGY
Homologene
FAMILY
  • cytochrome c oxidase subunit IV family
    • CATEGORY enzyme
    SUBCELLULAR LOCALIZATION     intracellular
    intracellular,cytoplasm,organelle,mitochondria,inner
    intracellular,cytoplasm,organelle,membrane
    basic FUNCTION
  • maybe participating in proton translocation
    • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
    protein
    cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) MTCO3 , LHON
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS