Statements (24)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:associatedWith |
gptkb:Leigh_syndrome
gptkb:MELAS_syndrome mitochondrial complex I deficiency |
| gptkbp:encodes |
NADH dehydrogenase 5 protein
|
| gptkbp:Entrez_Gene_ID |
4539
|
| gptkbp:fullName |
Mitochondrially encoded NADH dehydrogenase 5
|
| gptkbp:function |
electron transport
oxidative phosphorylation |
| gptkbp:HGNC_ID |
7457
|
| https://www.w3.org/2000/01/rdf-schema#label |
MT-ND5
|
| gptkbp:length |
1811 base pairs
|
| gptkbp:locatedIn |
gptkb:mitochondrial_DNA
|
| gptkbp:locatedOnChromosome |
gptkb:mitochondrial_chromosome
|
| gptkbp:mutationAssociatedWith |
mitochondrial disease
|
| gptkbp:OMIM |
516005
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:partOf |
gptkb:mitochondrial_respiratory_chain_complex_I
|
| gptkbp:strand |
heavy strand
|
| gptkbp:translatedInto |
gptkb:ND5_protein
|
| gptkbp:UniProtID |
gptkb:P03915
|
| gptkbp:bfsParent |
gptkb:NADH:ubiquinone_oxidoreductase_(Complex_I)
gptkb:NC_012920 |
| gptkbp:bfsLayer |
8
|