Statements (28)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:associatedWith |
mitochondrial ATP synthase complex
|
| gptkbp:encodes |
ATP synthase F0 subunit 8
|
| gptkbp:Entrez_Gene_ID |
4509
|
| gptkbp:function |
ATP synthesis
proton transport |
| gptkbp:hasTranscript |
NM_001256849.1
|
| gptkbp:HGNC_ID |
7471
|
| https://www.w3.org/2000/01/rdf-schema#label |
MT-ATP8
|
| gptkbp:inheritance |
maternally
|
| gptkbp:length |
207 base pairs
68 amino acids |
| gptkbp:locatedIn |
human mitochondrial DNA
|
| gptkbp:locatedOnChromosome |
mitochondrial
|
| gptkbp:mutationAssociatedWith |
gptkb:Leigh_syndrome
gptkb:mitochondrial_complex_V_deficiency neuromuscular disorders |
| gptkbp:neighboringGene |
gptkb:MT-CO3
gptkb:MT-ATP6 |
| gptkbp:OMIM |
516020
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:product |
NP_776772.1
|
| gptkbp:relatedTo |
mitochondrial diseases
|
| gptkbp:strand |
H-strand
|
| gptkbp:transcriptionDirection |
5' to 3'
|
| gptkbp:UniProtID |
P03923
|
| gptkbp:bfsParent |
gptkb:ATP_synthase
|
| gptkbp:bfsLayer |
7
|