Neogale vison (American mink): 122917769
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Entry
122917769 CDS
T08764
Name
(RefSeq) cytochrome c oxidase subunit 7C, mitochondrial
KO
K02272
cytochrome c oxidase subunit 7c
Organism
nvs
Neogale vison (American mink)
Pathway
nvs00190
Oxidative phosphorylation
nvs01100
Metabolic pathways
nvs04260
Cardiac muscle contraction
nvs04714
Thermogenesis
nvs04932
Non-alcoholic fatty liver disease
nvs05010
Alzheimer disease
nvs05012
Parkinson disease
nvs05014
Amyotrophic lateral sclerosis
nvs05016
Huntington disease
nvs05020
Prion disease
nvs05022
Pathways of neurodegeneration - multiple diseases
nvs05208
Chemical carcinogenesis - reactive oxygen species
nvs05415
Diabetic cardiomyopathy
Module
nvs_M00154
Cytochrome c oxidase
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
122917769
09150 Organismal Systems
09153 Circulatory system
04260 Cardiac muscle contraction
122917769
09159 Environmental adaptation
04714 Thermogenesis
122917769
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
122917769
09164 Neurodegenerative disease
05010 Alzheimer disease
122917769
05012 Parkinson disease
122917769
05014 Amyotrophic lateral sclerosis
122917769
05016 Huntington disease
122917769
05020 Prion disease
122917769
05022 Pathways of neurodegeneration - multiple diseases
122917769
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
122917769
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
122917769
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Motif
Pfam:
COX7C
Motif
Other DBs
NCBI-GeneID:
122917769
NCBI-ProteinID:
XP_044121971
UniProt:
A0A8C7ANK1
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Position
1:complement(205741013..205743369)
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AA seq
63 aa
AA seq
DB search
MLGQSIRRFTTSVVRRSHYEEGPGKNLPFSVENKWRLLVMMTLYFGSGFAAPFFIVRHQL
LKK
NT seq
192 nt
NT seq
+upstream
nt +downstream
nt
atgttgggacagagcatccggaggttcacaacctctgtggtccgtaggagccactatgag
gagggcccagggaagaatttgccattttcagtggaaaacaagtggcgattactagttatg
atgactttgtactttggatctggatttgctgcacctttttttatagtaagacatcaactg
cttaagaaataa
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