Statements (22)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:associatedWith |
mitochondrial translation
mitochondrial tRNA disorders |
| gptkbp:encodes |
tRNA-Val (transfer RNA for valine)
|
| gptkbp:Entrez_Gene_ID |
4579
ENSG00000210082 |
| gptkbp:fullName |
Mitochondrially encoded tRNA valine
|
| gptkbp:geneType |
tRNA gene
|
| gptkbp:HGNC_ID |
7492
|
| https://www.w3.org/2000/01/rdf-schema#label |
MT-TV
|
| gptkbp:locatedOnChromosome |
gptkb:mitochondrial_chromosome
|
| gptkbp:location |
human mitochondrial DNA
|
| gptkbp:mutationAssociatedWith |
gptkb:mitochondrial_DNA_depletion_syndrome
gptkb:mitochondrial_encephalomyopathy gptkb:mitochondrial_myopathy |
| gptkbp:OMIM |
590105
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:sequence |
72 nucleotides
|
| gptkbp:strand |
H-strand
|
| gptkbp:symbol |
gptkb:MT-TV
|
| gptkbp:bfsParent |
gptkb:NC_012920
|
| gptkbp:bfsLayer |
8
|