Entry |
|
Symbol |
COX3
|
Name |
cytochrome c oxidase subunit 3
|
Pathway |
map04932 | Non-alcoholic fatty liver disease |
map05022 | Pathways of neurodegeneration - multiple diseases |
map05208 | Chemical carcinogenesis - reactive oxygen species |
|
Module |
|
Disease |
H00068 | Leber hereditary optic atrophy |
H01368 | Cytochrome c oxidase (COX) deficiency |
|
Brite |
KEGG Orthology (KO) [BR:ko00001]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
K02262 COX3; cytochrome c oxidase subunit 3
09150 Organismal Systems
09153 Circulatory system
04260 Cardiac muscle contraction
K02262 COX3; cytochrome c oxidase subunit 3
09159 Environmental adaptation
04714 Thermogenesis
K02262 COX3; cytochrome c oxidase subunit 3
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
K02262 COX3; cytochrome c oxidase subunit 3
09164 Neurodegenerative disease
05010 Alzheimer disease
K02262 COX3; cytochrome c oxidase subunit 3
05012 Parkinson disease
K02262 COX3; cytochrome c oxidase subunit 3
05014 Amyotrophic lateral sclerosis
K02262 COX3; cytochrome c oxidase subunit 3
05016 Huntington disease
K02262 COX3; cytochrome c oxidase subunit 3
05020 Prion disease
K02262 COX3; cytochrome c oxidase subunit 3
05022 Pathways of neurodegeneration - multiple diseases
K02262 COX3; cytochrome c oxidase subunit 3
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
K02262 COX3; cytochrome c oxidase subunit 3
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
K02262 COX3; cytochrome c oxidase subunit 3
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis
K02262 COX3; cytochrome c oxidase subunit 3
Mitochondrial biogenesis [BR:ko03029]
Mitochondrial DNA transcription, translation, and replication factors
Mitochondrial DNA-encoded proteins
Cytochrome c oxidase
K02262 COX3; cytochrome c oxidase subunit 3
|
Other DBs |
|
Genes |
» show all
|
Reference |
|
Authors |
Johns DR, Neufeld MJ |
Title |
Cytochrome c oxidase mutations in Leber hereditary optic neuropathy. |
Journal |
|
Sequence |
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