KEGG   Homo sapiens (human): 9377
Entry
9377              CDS       T01001                                 
Symbol
COX5A, COX, COX-VA, MC4DN20, VA
Name
(RefSeq) cytochrome c oxidase subunit 5A
  KO
K02264  cytochrome c oxidase subunit 5a
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
    9377 (COX5A)
 09150 Organismal Systems
  09153 Circulatory system
   04260 Cardiac muscle contraction
    9377 (COX5A)
  09159 Environmental adaptation
   04714 Thermogenesis
    9377 (COX5A)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    9377 (COX5A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    9377 (COX5A)
   05012 Parkinson disease
    9377 (COX5A)
   05014 Amyotrophic lateral sclerosis
    9377 (COX5A)
   05016 Huntington disease
    9377 (COX5A)
   05020 Prion disease
    9377 (COX5A)
   05022 Pathways of neurodegeneration - multiple diseases
    9377 (COX5A)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    9377 (COX5A)
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    9377 (COX5A)
SSDB
Motif
Pfam: COX5A Anticodon_3
Other DBs
NCBI-GeneID: 9377
NCBI-ProteinID: NP_004246
OMIM: 603773
HGNC: 2267
Ensembl: ENSG00000178741
UniProt: P20674
Structure
Position
15:complement(74919791..74938073)
AA seq 150 aa
MLGAALRRCAVAATTRADPRGLLHSARTPGPAVAIQSVRCYSHGSQETDEEFDARWVTYF
NKPDIDAWELRKGINTLVTYDMVPEPKIIDAALRACRRLNDFASTVRILEVVKDKAGPHK
EIYPYVIQELRPTLNELGISTPEELGLDKV
NT seq 453 nt   +upstreamnt  +downstreamnt
atgctgggcgccgctctccgccgctgcgctgtggccgcaaccacccgggccgaccctcga
ggcctcctgcactccgcccggacccccggccccgccgtggctatccagtcagttcgctgc
tattcccatgggtcacaggagacagatgaggagtttgatgctcgctgggtaacatacttc
aacaagccagatatagatgcctgggaattgcgtaaagggataaacacacttgttacctat
gatatggttccagagcccaaaatcattgatgctgctttgcgggcatgcagacggttaaat
gattttgctagtacagttcgtatcctagaggttgttaaggacaaagcaggacctcataag
gaaatctacccctatgtcatccaggaacttagaccaactttaaatgaactgggaatctcc
actccggaggaactgggccttgacaaagtgtaa

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