Homo sapiens (human): 51241
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Entry
51241 CDS
T01001
Symbol
COX16, C14orf112, HSPC203, MC4DN22, hCOX16
Name
(RefSeq) cytochrome c oxidase assembly factor COX16
KO
K18182
cytochrome c oxidase assembly protein subunit 16
Organism
hsa
Homo sapiens (human)
Pathway
hsa04714
Thermogenesis
Network
nt06529
Thermogenesis
Element
N01691
mitochondrial complex - UCP1 in Thermogenesis
Disease
H01368
Cytochrome c oxidase (COX) deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09159 Environmental adaptation
04714 Thermogenesis
51241 (COX16)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
51241 (COX16)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial quality control factors
Mitochondrial respiratory chain complex assembly factors
Complex-IV assembly factors
51241 (COX16)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
COX16
TubC_N
AcrIC5
Motif
Other DBs
NCBI-GeneID:
51241
NCBI-ProteinID:
NP_057552
OMIM:
618064
HGNC:
20213
Ensembl:
ENSG00000133983
UniProt:
Q9P0S2
LinkDB
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Position
14:complement(70325081..70359683)
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AA seq
106 aa
AA seq
DB search
MFAPAVMRAFRKNKTLGYGVPMLLLIVGGSFGLREFSQIRYDAVKSKMDPELEKKLKENK
ISLESEYEKIKDSKFDDWKNIRGPRPWEDPDLLQGRNPESLKTKTT
NT seq
321 nt
NT seq
+upstream
nt +downstream
nt
atgtttgcacccgcggtgatgcgtgcttttcgcaagaacaagactctcggctatggagtc
cccatgttgttgctgattgttggaggttcttttggtcttcgtgagttttctcaaatccga
tatgatgctgtgaagagtaaaatggatcctgagcttgaaaaaaaactgaaagagaataaa
atatctttagagtcggaatatgagaaaatcaaagactccaagtttgatgactggaagaat
attcgaggacccaggccttgggaagatcctgacctcctccaaggaagaaatccagaaagc
cttaagactaagacaacttga
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integrated database retrieval system