Statements (27)
Predicate | Object |
---|---|
gptkbp:instanceOf |
gptkb:gene
|
gptkbp:alternativeName |
gptkb:MT-ATP6
gptkb:ATP_synthase_F0_subunit_6 gptkb:ATPase6 |
gptkbp:associatedWith |
gptkb:Leigh_syndrome
gptkb:NARP_syndrome gptkb:mitochondrial_complex_V_deficiency |
gptkbp:encodes |
gptkb:ATP_synthase_subunit_a
|
gptkbp:Entrez_Gene_ID |
4509
|
gptkbp:fullName |
Mitochondrially encoded ATP synthase membrane subunit 6
|
gptkbp:function |
component of ATP synthase (Complex V)
involved in ATP production |
gptkbp:geneType |
protein-coding
|
gptkbp:HGNC_ID |
7411
|
https://www.w3.org/2000/01/rdf-schema#label |
MTATP6
|
gptkbp:length |
681 base pairs
|
gptkbp:locatedOnChromosome |
gptkb:mitochondrial_chromosome
|
gptkbp:location |
gptkb:mitochondrial_DNA
|
gptkbp:mutationAssociatedWith |
can cause mitochondrial diseases
|
gptkbp:numberOfExons |
1
|
gptkbp:OMIM |
516060
|
gptkbp:organism |
gptkb:Homo_sapiens
|
gptkbp:strand |
heavy strand
|
gptkbp:transcription |
poly-cistronic transcript with MTATP8
|
gptkbp:UniProtID |
P00846
|
gptkbp:bfsParent |
gptkb:MT-ATP6
|
gptkbp:bfsLayer |
8
|