Homo sapiens (human): 1339
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Entry
1339 CDS
T01001
Symbol
COX6A2, COX6AH, COXVIAH, COXVIa-M, MC4DN18
Name
(RefSeq) cytochrome c oxidase subunit 6A2
KO
K02266
cytochrome c oxidase subunit 6a
Organism
hsa
Homo sapiens (human)
Pathway
hsa00190
Oxidative phosphorylation
hsa01100
Metabolic pathways
hsa04260
Cardiac muscle contraction
hsa04714
Thermogenesis
hsa04932
Non-alcoholic fatty liver disease
hsa05010
Alzheimer disease
hsa05012
Parkinson disease
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05020
Prion disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05208
Chemical carcinogenesis - reactive oxygen species
hsa05415
Diabetic cardiomyopathy
Module
hsa_M00154
Cytochrome c oxidase
Network
nt06252
Mitochondrial ROS formation (cancer)
nt06460
Alzheimer disease
nt06466
Pathways of neurodegeneration
nt06529
Thermogenesis
Element
N00998
Electron transfer in Complex IV
N00999
Mutation-caused aberrant Abeta to electron transfer in Complex IV
N01394
Arsenic to electron transfer in complex IV
N01691
mitochondrial complex - UCP1 in Thermogenesis
Disease
H01368
Cytochrome c oxidase (COX) deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
1339 (COX6A2)
09150 Organismal Systems
09159 Environmental adaptation
04714 Thermogenesis
1339 (COX6A2)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
1339 (COX6A2)
09164 Neurodegenerative disease
05010 Alzheimer disease
1339 (COX6A2)
05012 Parkinson disease
1339 (COX6A2)
05014 Amyotrophic lateral sclerosis
1339 (COX6A2)
05016 Huntington disease
1339 (COX6A2)
05020 Prion disease
1339 (COX6A2)
05022 Pathways of neurodegeneration - multiple diseases
1339 (COX6A2)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
1339 (COX6A2)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
1339 (COX6A2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
COX6A
Motif
Other DBs
NCBI-GeneID:
1339
NCBI-ProteinID:
NP_005196
OMIM:
602009
HGNC:
2279
Ensembl:
ENSG00000156885
Pharos:
Q02221
(Tbio)
UniProt:
Q02221
LinkDB
All DBs
Position
16:complement(31427731..31428360)
Genome browser
AA seq
97 aa
AA seq
DB search
MALPLRPLTRGLASAAKGGHGGAGARTWRLLTFVLALPSVALCTFNSYLHSGHRPRPEFR
PYQHLRIRTKPYPWGDGNHTLFHNSHVNPLPTGYEHP
NT seq
294 nt
NT seq
+upstream
nt +downstream
nt
atggctttgcctctgaggcccctgacccggggcttggccagcgctgccaaaggaggccac
ggaggagcaggagctcgtacctggcgtctgctgaccttcgtgctggcgctgcccagcgtg
gccctctgcaccttcaactcctatctccactcgggccaccgcccgcgccccgagttccgt
ccctaccaacacctccgcatccgcaccaagccctacccctggggggacggcaaccacact
ctgttccacaatagccacgtgaaccctctgcccacgggctacgaacacccctga
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integrated database retrieval system