Statements (25)
Predicate | Object |
---|---|
gptkbp:instanceOf |
gptkb:gene
|
gptkbp:associatedWith |
gptkb:Leigh_syndrome
gptkb:Leber's_hereditary_optic_neuropathy gptkb:mitochondrial_encephalomyopathy |
gptkbp:encodes |
gptkb:NADH_dehydrogenase_6_protein
|
gptkbp:Entrez_Gene_ID |
4541
|
gptkbp:fullName |
Mitochondrially encoded NADH dehydrogenase 6
|
gptkbp:function |
electron transport
oxidative phosphorylation |
gptkbp:HGNC_ID |
7457
|
https://www.w3.org/2000/01/rdf-schema#label |
MT-ND6
|
gptkbp:locatedIn |
gptkb:mitochondrial_DNA
|
gptkbp:locatedOnChromosome |
gptkb:mitochondrial_chromosome
|
gptkbp:mutationAssociatedWith |
mitochondrial disease
|
gptkbp:OMIM |
516006
|
gptkbp:organism |
gptkb:Homo_sapiens
|
gptkbp:partOf |
gptkb:mitochondrial_respiratory_chain_complex_I
|
gptkbp:sequence |
525 base pairs
|
gptkbp:strand |
light strand
|
gptkbp:translatedInto |
174 amino acids
|
gptkbp:UniProtID |
P03923
|
gptkbp:bfsParent |
gptkb:Leber's_hereditary_optic_neuropathy
gptkb:NADH:ubiquinone_oxidoreductase_(Complex_I) gptkb:NC_012920 |
gptkbp:bfsLayer |
8
|