KEGG   Homo sapiens (human): 1347
Entry
1347              CDS       T01001                                 
Symbol
COX7A2, COX7AL, COX7AL1, COXVIIAL, COXVIIa-L, VIIAL
Name
(RefSeq) cytochrome c oxidase subunit 7A2
  KO
K02270  cytochrome c oxidase subunit 7a
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
  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
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09100 Metabolism
  09102 Energy metabolism
   00190 Oxidative phosphorylation
    1347 (COX7A2)
 09150 Organismal Systems
  09153 Circulatory system
   04260 Cardiac muscle contraction
    1347 (COX7A2)
  09159 Environmental adaptation
   04714 Thermogenesis
    1347 (COX7A2)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    1347 (COX7A2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    1347 (COX7A2)
   05012 Parkinson disease
    1347 (COX7A2)
   05014 Amyotrophic lateral sclerosis
    1347 (COX7A2)
   05016 Huntington disease
    1347 (COX7A2)
   05020 Prion disease
    1347 (COX7A2)
   05022 Pathways of neurodegeneration - multiple diseases
    1347 (COX7A2)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    1347 (COX7A2)
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    1347 (COX7A2)
SSDB
Motif
Pfam: COX7a
Other DBs
NCBI-GeneID: 1347
NCBI-ProteinID: NP_001856
OMIM: 123996
HGNC: 2288
Ensembl: ENSG00000112695
UniProt: P14406 H0UI06
Structure
Position
6:complement(75237675..75250298)
AA seq 83 aa
MLRNLLALRQIGQRTISTASRRHFKNKVPEKQKLFQEDDEIPLYLKGGVADALLYRATMI
LTVGGTAYAIYELAVASFPKKQE
NT seq 252 nt   +upstreamnt  +downstreamnt
atgctgcggaatctgctggctcttcgtcagattgggcagaggacgataagcactgcttcc
cgcaggcattttaaaaataaagttccggagaagcaaaaactgttccaggaggatgatgaa
attccactgtatctaaagggtggggtagctgatgccctcctgtatagagccaccatgatt
cttacagttggtggaacagcatatgccatatatgagctggctgtggcttcatttcccaag
aagcaggagtga

  All links  
Ontology (1)   
   KEGG BRITE (1)   
Pathway (14)   
   KEGG PATHWAY (13)   
   KEGG MODULE (1)   
Network (6)   
   KEGG NETWORK (6)   
Disease (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (32)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (25)   
   OC (1)   
Protein sequence (12)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (9)   
DNA sequence (42)   
   RefSeq(nuc) (12)   
   GenBank (15)   
   EMBL (15)   
3D Structure (1)   
   PDB (1)   
Protein domain (1)   
   Pfam (1)   
All databases (111)   

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