|
gptkbp:instanceOf
|
gptkb:gene
|
|
gptkbp:alternativeTo
|
gptkb:COX2
COII
|
|
gptkbp:associatedWith
|
gptkb:Leigh_syndrome
gptkb:mitochondrial_complex_IV_deficiency
muscular dystrophy
|
|
gptkbp:discoveredIn
|
1981
|
|
gptkbp:encodes
|
cytochrome c oxidase subunit II
|
|
gptkbp:Entrez_Gene_ID
|
4513
ENSG00000198712
|
|
gptkbp:expressedIn
|
all human tissues
|
|
gptkbp:fullName
|
Mitochondrially encoded cytochrome c oxidase II
|
|
gptkbp:function
|
oxidative phosphorylation
electron transport chain
|
|
gptkbp:gene
|
gptkb:MT-CO2
|
|
gptkbp:geneType
|
protein-coding
|
|
gptkbp:GO_term
|
gptkb:GO:0004129
gptkb:GO:0005739
GO:0006119
|
|
gptkbp:HGNC_ID
|
7412
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
MT-CO2
|
|
gptkbp:inheritance
|
maternally
|
|
gptkbp:locatedOnChromosome
|
gptkb:mitochondrial_chromosome
|
|
gptkbp:location
|
human mitochondrial DNA
|
|
gptkbp:mutationAssociatedWith
|
nonsense
deletion
insertion
missense
mitochondrial disease
|
|
gptkbp:numberOfExons
|
1
|
|
gptkbp:OMIM
|
516040
|
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
|
gptkbp:orthologIn
|
mouse Mt-co2
rat Mt-co2
|
|
gptkbp:pathway
|
electron transport chain
oxidative phosphorylation pathway
|
|
gptkbp:product
|
gptkb:COX2
|
|
gptkbp:protein_complex
|
gptkb:cytochrome_c_oxidase_(Complex_IV)
|
|
gptkbp:protein_length_(aa)
|
227
|
|
gptkbp:proteinFamily
|
gptkb:mitochondrial_respiratory_chain_complex_IV
|
|
gptkbp:RefSeq
|
gptkb:NC_012920.1
NP_004018.2
|
|
gptkbp:relatedTo
|
ATP synthesis
cellular respiration
|
|
gptkbp:sequence_accession
|
NC_012920.1:7586-8269
|
|
gptkbp:strand
|
heavy strand
|
|
gptkbp:subcellularLocation
|
mitochondrion inner membrane
|
|
gptkbp:transcript_length_(nt)
|
684
|
|
gptkbp:UniProtID
|
P00403
|
|
gptkbp:bfsParent
|
gptkb:P00338
gptkb:P03891
gptkb:NC_012920
|
|
gptkbp:bfsLayer
|
8
|