KEGG   Homo sapiens (human): 388753
Entry
388753            CDS       T01001                                 
Symbol
COA6, C1orf31, CEMCOX4, MC4DN13
Name
(RefSeq) cytochrome c oxidase assembly factor 6
  KO
K18179  cytochrome c oxidase assembly factor 6
Organism
hsa  Homo sapiens (human)
Pathway
hsa04714  Thermogenesis
Network
nt06529  Thermogenesis
  Element
N01691  mitochondrial complex - UCP1 in Thermogenesis
Disease
H01200  Fatal infantile cardioencephalomyopathy
H01368  Cytochrome c oxidase (COX) deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09159 Environmental adaptation
   04714 Thermogenesis
    388753 (COA6)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    388753 (COA6)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial quality control factors
  Mitochondrial respiratory chain complex assembly factors
   Complex-IV assembly factors
    388753 (COA6)
SSDB
Motif
Pfam: COX6B CHCH Lepto_8Cys Pet191_N
Other DBs
NCBI-GeneID: 388753
NCBI-ProteinID: NP_001013003
OMIM: 614772
HGNC: 18025
Ensembl: ENSG00000168275
UniProt: Q5JTJ3
Structure
LinkDB
Position
1:234373456..234385080
AA seq 125 aa
MGPGGPLLSPSRGFLLCKTGWHSNRLLGDCGPHTPVSTALSFIAVGMAAPSMKERQVCWG
ARDEYWKCLDENLEDASQCKKLRSSFESSCPQQWIKYFDKRRDYLKFKEKFEAGQFEPSE
TTAKS
NT seq 378 nt   +upstreamnt  +downstreamnt
atgggcccgggaggtcccttactgtccccgagccgcgggttcctcttgtgcaaaacgggg
tggcactccaatcgcctgcttggtgattgtggcccccacacacctgtttctacagcgctt
agcttcatcgcagtaggaatggcagccccatctatgaaggaaagacaggtctgctggggg
gcccgggatgagtactggaagtgtttagatgagaacttagaggatgcttctcaatgcaag
aagttaagaagctctttcgaatcaagttgtccccaacagtggataaaatattttgataaa
agaagagactacttaaaattcaaagaaaaatttgaagcaggacaatttgagccttcagaa
acaactgcaaaatcctag

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