Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:associatedWith |
mitochondrial diseases
|
| gptkbp:component |
gptkb:Complex_I
|
| gptkbp:encodes |
gptkb:NADH_dehydrogenase_(ubiquinone)_1_beta_subcomplex_subunit_2
|
| gptkbp:foundIn |
gptkb:Homo_sapiens
many eukaryotes |
| gptkbp:fullName |
gptkb:NADH_dehydrogenase_subunit_2
|
| gptkbp:gene |
gptkb:MT-ND2
|
| https://www.w3.org/2000/01/rdf-schema#label |
ND2
|
| gptkbp:involvedIn |
oxidative phosphorylation
|
| gptkbp:locatedIn |
gptkb:mitochondrial_DNA
|
| gptkbp:locatedOnChromosome |
gptkb:mitochondrial_chromosome
|
| gptkbp:mutationAssociatedWith |
gptkb:Leber's_hereditary_optic_neuropathy
gptkb:MELAS_syndrome mitochondrial complex I deficiency |
| gptkbp:OMIM |
516001
|
| gptkbp:product |
gptkb:ND2_protein
|
| gptkbp:RefSeq |
gptkb:NC_012920.1
|
| gptkbp:sequence |
1041 base pairs
|
| gptkbp:strand |
heavy strand
|
| gptkbp:UniProtID |
gptkb:P03891
|
| gptkbp:bfsParent |
gptkb:Mitochondrial_Complex_I_protein
|
| gptkbp:bfsLayer |
6
|