Homo sapiens (human): 1340
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Entry
1340 CDS
T01001
Symbol
COX6B1, COX6B, COXG, COXVIb1, MC4DN7
Name
(RefSeq) cytochrome c oxidase subunit 6B1
KO
K02267
cytochrome c oxidase subunit 6b
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
1340 (COX6B1)
09150 Organismal Systems
09153 Circulatory system
04260 Cardiac muscle contraction
1340 (COX6B1)
09159 Environmental adaptation
04714 Thermogenesis
1340 (COX6B1)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
1340 (COX6B1)
09164 Neurodegenerative disease
05010 Alzheimer disease
1340 (COX6B1)
05012 Parkinson disease
1340 (COX6B1)
05014 Amyotrophic lateral sclerosis
1340 (COX6B1)
05016 Huntington disease
1340 (COX6B1)
05020 Prion disease
1340 (COX6B1)
05022 Pathways of neurodegeneration - multiple diseases
1340 (COX6B1)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
1340 (COX6B1)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
1340 (COX6B1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
COX6B
YozE_SAM_like
Motif
Other DBs
NCBI-GeneID:
1340
NCBI-ProteinID:
NP_001854
OMIM:
124089
HGNC:
2280
Ensembl:
ENSG00000126267
Pharos:
P14854
(Tbio)
UniProt:
P14854
Structure
PDB
PDBj
LinkDB
All DBs
Position
19:35648323..35658782
Genome browser
AA seq
86 aa
AA seq
DB search
MAEDMETKIKNYKTAPFDSRFPNQNQTRNCWQNYLDFHRCQKAMTAKGGDISVCEWYQRV
YQSLCPTSWVTDWDEQRAEGTFPGKI
NT seq
261 nt
NT seq
+upstream
nt +downstream
nt
atggcggaagacatggagaccaaaatcaagaactacaagaccgccccttttgacagccgc
ttccccaaccagaaccagactagaaactgctggcagaactacctggacttccaccgctgt
cagaaggcaatgaccgctaaaggaggcgatatctctgtgtgcgaatggtaccagcgtgtg
taccagtccctctgccccacatcctgggtcacagactgggatgagcaacgggctgaaggc
acgtttcccgggaagatctga
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