Mustela nigripes (black-footed ferret): 20466141
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Entry
20466141 CDS
T09425
Symbol
COX2
Name
(RefSeq) cytochrome c oxidase subunit II
KO
K02261
cytochrome c oxidase subunit 2
Organism
mnp
Mustela nigripes (black-footed ferret)
Pathway
mnp00190
Oxidative phosphorylation
mnp01100
Metabolic pathways
mnp04260
Cardiac muscle contraction
mnp04714
Thermogenesis
mnp04932
Non-alcoholic fatty liver disease
mnp05010
Alzheimer disease
mnp05012
Parkinson disease
mnp05014
Amyotrophic lateral sclerosis
mnp05016
Huntington disease
mnp05020
Prion disease
mnp05022
Pathways of neurodegeneration - multiple diseases
mnp05208
Chemical carcinogenesis - reactive oxygen species
mnp05415
Diabetic cardiomyopathy
Module
mnp_M00154
Cytochrome c oxidase
Brite
KEGG Orthology (KO) [BR:
mnp00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
20466141 (COX2)
09150 Organismal Systems
09153 Circulatory system
04260 Cardiac muscle contraction
20466141 (COX2)
09159 Environmental adaptation
04714 Thermogenesis
20466141 (COX2)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
20466141 (COX2)
09164 Neurodegenerative disease
05010 Alzheimer disease
20466141 (COX2)
05012 Parkinson disease
20466141 (COX2)
05014 Amyotrophic lateral sclerosis
20466141 (COX2)
05016 Huntington disease
20466141 (COX2)
05020 Prion disease
20466141 (COX2)
05022 Pathways of neurodegeneration - multiple diseases
20466141 (COX2)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
20466141 (COX2)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
20466141 (COX2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
mnp03029
]
20466141 (COX2)
Mitochondrial biogenesis [BR:
mnp03029
]
Mitochondrial DNA transcription, translation, and replication factors
Mitochondrial DNA-encoded proteins
Cytochrome c oxidase
20466141 (COX2)
BRITE hierarchy
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
COX2
COX2_TM
Oxidored_q3
T2SSI
Motif
Other DBs
NCBI-GeneID:
20466141
NCBI-ProteinID:
YP_009059652
UniProt:
A0A0U1XAQ3
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Position
MT:7024..7707
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AA seq
227 aa
AA seq
DB search
MAYPFQMGLQDAASPIMEELLHFHDHTLMIVFLISSLVLYIISVMLTTKLTHTSTMDAQA
VETIWTILPAIILIMIALPSLRILYMMDEINNPSLTVKTMGHQWYWSYEYTDYEDLNFDS
YMIPTQELKPGELRLLEVDNRVVLPMEMTIRMLISSEDVLHSWAVPSLGLKTDAIPGRLN
QTTIMAMRPGLYYGQCSEICGSNHSFMPIVLELVPLSYFEKWSASML
NT seq
684 nt
NT seq
+upstream
nt +downstream
nt
atggcgtaccctttccaaataggcctccaagatgcagcctctcctatcatagaggaactt
ctacactttcacgatcacacattaataattgtatttctaattagttctcttgtactttac
attatttcagtaatactaactaccaagcttacgcatacaagtaccatagacgcccaagca
gttgaaacaatctgaaccatcctaccagccattattttgatcataatcgctctaccctct
ctacgaattctctatatgatagacgagatcaacaacccctctttaaccgtaaaaactatg
ggtcaccaatgatactgaagttatgaatatacagactacgaagacttaaacttcgactcc
tacataatcccaactcaagaactgaaaccaggggaactacgacttctagaagtggacaat
cgagtagtgctcccaatagaaataacaattcgtatactaatttcttctgaggacgtatta
cactcatgagccgtcccatccctaggattaaaaactgatgctatcccaggacgccttaac
caaactactattatagccatacgaccgggattatactacggccaatgctctgaaatctgc
ggctctaatcacagcttcatacccattgtcctcgagctagtacctttatcatacttcgaa
aaatgatctgcctcaatactataa
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