GTPBP3 (GTP binding protein 3, mitochondrial)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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84705 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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GTP binding protein 3, mitochondrial |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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GTPBP3 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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COXPD23, GTPBG3, MSS1, MTGP1, THDF1 |
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Chromosome
Chromosome number
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19 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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19p13.11 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This locus encodes a GTP-binding protein. The encoded protein is localized to the mitochondria and may play a role in mitochondrial tRNA modification. Polymorphisms at this locus may be associated with severity of aminoglycoside-induced deafness, a diseas |
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SNPs
SNP information provided by dbSNP.
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||||||||||||
| UniProt ID | Q969Y2 | ||||||||||||||||||||
| Protein name | 5-taurinomethyluridine-[tRNA] synthase subunit GTPB3, mitochondrial (EC 3.6.1.-) (GTP-binding protein 3) (Mitochondrial GTP-binding protein 1) (tRNA modification GTPase GTPBP3, mitochondrial) | ||||||||||||||||||||
| Protein function | GTPase component of the GTPBP3-MTO1 complex that catalyzes the 5-taurinomethyluridine (taum(5)U) modification at the 34th wobble position (U34) of mitochondrial tRNAs (mt-tRNAs), which plays a role in mt-tRNA decoding and mitochondrial translati | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Ubiquitously expressed. {ECO:0000269|PubMed:12370316}. | ||||||||||||||||||||
| Sequence | |||||||||||||||||||||
| Sequence length | 492 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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