KEGG   Homo sapiens (human): 9167
Entry
9167              CDS       T01001                                 
Symbol
COX7A2L, COX7AR, COX7RP, EB1, SCAF1, SCAFI, SIG81
Name
(RefSeq) cytochrome c oxidase subunit 7A2 like
  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
    9167 (COX7A2L)
 09150 Organismal Systems
  09153 Circulatory system
   04260 Cardiac muscle contraction
    9167 (COX7A2L)
  09159 Environmental adaptation
   04714 Thermogenesis
    9167 (COX7A2L)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    9167 (COX7A2L)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    9167 (COX7A2L)
   05012 Parkinson disease
    9167 (COX7A2L)
   05014 Amyotrophic lateral sclerosis
    9167 (COX7A2L)
   05016 Huntington disease
    9167 (COX7A2L)
   05020 Prion disease
    9167 (COX7A2L)
   05022 Pathways of neurodegeneration - multiple diseases
    9167 (COX7A2L)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    9167 (COX7A2L)
  09167 Endocrine and metabolic disease
   04932 Non-alcoholic fatty liver disease
    9167 (COX7A2L)
SSDB
Motif
Pfam: COX7a
Other DBs
NCBI-GeneID: 9167
NCBI-ProteinID: NP_001305965
OMIM: 605771
HGNC: 2289
Ensembl: ENSG00000115944
UniProt: O14548 Q6FGA0
Position
2:complement(42335559..42368957)
AA seq 114 aa
MYYKFSGFTQKLAGAWASEAYSPQGLKPVVSTEAPPIIFATPTKLTSDSTVYDYAGKNKV
PELQKFFQKADGVPVYLKRGLPDQMLYRTTMALTVGGTIYCLIALYMASQPKNK
NT seq 345 nt   +upstreamnt  +downstreamnt
atgtactacaagtttagtggcttcacgcagaagttggcaggagcatgggcttcggaggcc
tatagcccgcagggattaaagcctgtggtttccacagaagcaccacctatcatatttgcc
acaccaactaaactgacctccgattccacagtgtatgattatgctgggaaaaacaaagtt
ccagagctacaaaagtttttccagaaagctgatggtgtgcccgtctacctgaaacgaggc
ctgcctgaccaaatgctttaccggaccaccatggcgctgactgtgggagggaccatctac
tgcctgatcgccctctacatggcttcgcagcccaaaaacaaatga

  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 (24)   
   KEGG ORTHOLOGY (1)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (16)   
   OC (1)   
Protein sequence (10)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (7)   
DNA sequence (37)   
   RefSeq(nuc) (9)   
   GenBank (14)   
   EMBL (14)   
Protein domain (1)   
   Pfam (1)   
All databases (95)   

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