MT-CO1 - mitochondrially encoded cytochrome c oxidase I Gene
Also Known as COI; MTCO1; COX1
Species: Homo sapiens
Summary
Contributes to cytochrome-c oxidase activity. Predicted to be involved in electron transport coupled proton transport and mitochondrial electron transport, cytochrome c to oxygen. Part of mitochondrial respiratory chain complex III and mitochondrial respiratory chain complex IV. [provided by Alliance of Genome Resources, Apr 2022]
MT-CO1 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| YP_003024028.1 cytochrome c oxidase subunit I (mitochondrion) [Homo sapiens] |
| Molecular Function GO Annotation | Evidence | Références | Source |
|---|---|---|---|
| contributes to cytochrome-c oxidase activity |
IMP
IMP: Inferred from mutant phenotype
|
12140182 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
12762840 | GOA |
| Cellular Component GO Annotation | Evidence | Références | Source |
|---|---|---|---|
| located in mitochondrial membrane |
IDA
IDA: Inferred from direct assay
|
30030519 | GOA |
| part of respiratory chain complex IV |
IDA
IDA: Inferred from direct assay
|
1651240 | GOA |
| part of respiratory chain complex IV |
IMP
IMP: Inferred from mutant phenotype
|
19393246 | GOA |
MT-CO1 Protein Structure
COX1: Cytochrome C and Quinol oxidase polypeptide I (12 - 460)
- 0
- 100
- 200
- 300
- 400
- 513 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
cytochrome c oxidase subunit I |
|
MT-CO1 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | Références |
|---|---|---|---|---|---|---|---|
|
Intra
|
MT-CO1 | P00395 | COX4I1 | Homo sapiens | P13073 | 23260140 | |
|
Intra
|
MT-CO1 | P00395 | COA3 | Homo sapiens | Q9Y2R0 | 23260140 | |
|
Intra
|
MT-CO1 | P00395 | COA3 | Homo sapiens | Q9Y2R0 | 23260140 | |
|
Intra
|
MT-CO1 | P00395 | TIMM21 | Homo sapiens | Q9BVV7 | 23260140 |
MT-CO1 Anticorps
| Cat. No. | Nom du produit | Application | Reactivity |
|---|---|---|---|
| HY-P86965 | MTCO1 Antibody (YA6658) | WB, ICC/IF, IHC-P, FC, IF-Tissue | Human, Mouse, Rat |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Deafness, Nonsyndromic Sensorineural, Mitochondrial |
|
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| Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 |
|
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| Myoglobinuria, Recurrent |
|
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| Mitochondrial Complex Iv Deficiency, Nuclear Type 1 |
|
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| Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes |
|
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| Genetic Recurrent Myoglobinuria |
|
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| Keratoderma, Palmoplantar, With Deafness |
|
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| Familial Colorectal Cancer |
|
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| Tetralogy Of Fallot |
|
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| Leber Hereditary Optic Neuropathy, Modifier Of |
|
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| Isolated Cytochrome C Oxidase Deficiency |
|
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| Leber Plus Disease |
|
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| Colorectal Cancer |
|
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| Echinococcosis |
|
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| Leigh Syndrome |
|
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| Mitochondrial Myopathy, Infantile, Transient |
|
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| Myoglobinuria |
|
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| Sparganosis |
|
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| Myiasis |
|
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| Parasitic Ectoparasitic Infectious Disease |
|
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| Taeniasis |
|
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| Diphyllobothriasis |
|
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| Neonatal Candidiasis |
|
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| Metagonimiasis |
|
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| Setariasis |
|
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| Gnathomiasis |
|
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| Sarcocystosis |
|
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| Angiostrongyliasis |
|
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| Acanthocephaliasis |
|
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| Tick Infestation |
|
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| Dioctophymiasis |
|
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| Thelaziasis |
|
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| Sideroblastic Anemia |
|
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| Mesocestoidiasis |
|
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| Ophthalmomyiasis |
|
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| Coenurosis |
|
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| Tick Paralysis |
|
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| Eosinophilic Meningitis |
|
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| Cercarial Dermatitis |
|
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| Dirofilariasis |
|
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| Hymenolepiasis |
|
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| Leech Infestation |
|
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| Oesophagostomiasis |
|
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| Cystic Echinococcosis |
|
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| Ancylostomiasis |
|
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| Epidemic Typhus |
|
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| Dipetalonemiasis |
|
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| Enterobiasis |
|
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| Dientamoebiasis |
|
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| Adenosquamous Bile Duct Carcinoma |
|
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| Alveolar Echinococcosis |
|
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| Nemaline Myopathy 3 |
|
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| Lice Infestation |
|
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| Echinostomiasis |
|
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| Parasitic Helminthiasis Infectious Disease |
|
|
| Chronic Meningitis |
|
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| Polycystic Echinococcosis |
|
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| Mite Infestation |
|
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| Babesiosis |
|
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| Paragonimiasis |
|
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| Cystoisosporiasis |
|
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| Pediculus Humanus Capitis Infestation |
|
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| Neuropathy |
|
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| Clivus Meningioma |
|
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| Dracunculiasis |
|
|
| Pediculus Humanus Corporis Infestation |
|
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| Capillariasis |
|
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| Mitochondrial Myopathy |
|
|
| Baylisascariasis |
|
|
| Cysticercosis |
|
|
| Kearns-Sayre Syndrome |
|
|
| Bartonellosis |
|
|
| Filarial Elephantiasis |
|
|
| Theileriasis |
|
|
| Phlebotomus Fever |
|
|
| Strongyloidiasis |
|
|
| Fascioliasis |
|
|
| Epilepsy, Familial Temporal Lobe, 2 |
|
|
| Slate Pneumoconiosis |
|
|
| Hypertrophic Cardiomyopathy |
|
|
| Trench Fever |
|
|
| Motor Neuron Disease |
|
|
| Endemic Typhus |
|
|
| Holoprosencephaly 1 |
|
|
| Norwegian Scabies |
|
|
| Squamous Cell Bile Duct Carcinoma |
|
|
| Osteogenesis Imperfecta, Type Xiii |
|
|
| Filariasis |
|
|
| Eastern Equine Encephalitis |
|
|
| Intestinal Schistosomiasis |
|
|
| Deafness, Aminoglycoside-Induced |
|
|
| Parasitic Protozoa Infectious Disease |
|
|
| Autoimmune Lymphoproliferative Syndrome |
|
|
| Clonorchiasis |
|
|
| Spotted Fever |
|
|
| Chronic Progressive External Ophthalmoplegia |
|
|
| Sensorineural Hearing Loss |
|
|
| Mitochondrial Encephalomyopathy |
|
|
| Huntington Disease |
|
|
| Parathyroid Oncocytic Adenoma |
|
|
| Hypersensitivity Reaction Type Iv Disease |
|
|
| Articulation Disorder |
|
|
| Myopathy, Lactic Acidosis, And Sideroblastic Anemia 3 |
|
|
| Chronic Congestive Splenomegaly |
|
|
| Combined Oxidative Phosphorylation Deficiency 37 |
|
|
| 3-Methylglutaconic Aciduria, Type Iii |
|
|
| Osebold-Remondini Syndrome |
|
|
| Myopathy |
|
|
| Stuttering |
|
|
| Mitochondrial Dna Depletion Syndrome |
|
|
| Trombiculiasis |
|
|
| Malaria |
|
|
| Osteogenesis Imperfecta, Type Xi |
|
|
| Psoriasis 11 |
|
|
| Meningovascular Neurosyphilis |
|
|
| Optic Nerve Disease |
|
|
| Myoclonic Epilepsy Associated With Ragged-Red Fibers |
|
|
| Lactic Acidosis |
|
|
| Hypertension, Essential |
|
|
| Mitochondrial Complex I Deficiency, Nuclear Type 1 |
|
|
| Nervous System Disease |
|
|