Statements (21)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alternativeName |
gptkb:Complex_I_subunit_NDUFS4
CI-49kD |
| gptkbp:associatedWith |
gptkb:Leigh_syndrome
mitochondrial complex I deficiency |
| gptkbp:component |
gptkb:mitochondrial_complex_I
|
| gptkbp:encodes |
gptkb:NADH_dehydrogenase_[ubiquinone]_iron-sulfur_protein_4,_mitochondrial
|
| gptkbp:Entrez_Gene_ID |
4724
|
| gptkbp:expressedIn |
mitochondria
|
| gptkbp:function |
oxidative phosphorylation
electron transport chain |
| gptkbp:HGNC_ID |
HGNC:7700
|
| https://www.w3.org/2000/01/rdf-schema#label |
NDUFS4
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_5
gptkb:5q11.2 |
| gptkbp:mutationAssociatedWith |
mitochondrial dysfunction
|
| gptkbp:OMIM |
602694
|
| gptkbp:orthologInMouse |
gptkb:Ndufs4
|
| gptkbp:UniProtID |
O43181
|
| gptkbp:bfsParent |
gptkb:Mitochondrial_Complex_I_protein
|
| gptkbp:bfsLayer |
6
|