XB-FEAT-944602: Difference between revisions
imported>Xenbase gene generator No edit summary |
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This is the community wiki page for the gene ''nars2'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | This is the community wiki page for the gene ''nars2'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=nomenclature changes= | |||
09/24/2017 | |||
Human name has changed for Entrez Gene: 79731. From asparaginyl-tRNA synthetase 2, mitochondrial (putative) to asparaginyl-tRNA synthetase 2, mitochondrial | |||
=summary from NCBI= | |||
This gene encodes a putative member of the class II family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of asparagine to tRNA molecules. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency 24 (COXPD24). [provided by RefSeq, Mar 2015] | |||
Latest revision as of 10:11, 27 September 2017
nars2
This is the community wiki page for the gene nars2 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
09/24/2017 Human name has changed for Entrez Gene: 79731. From asparaginyl-tRNA synthetase 2, mitochondrial (putative) to asparaginyl-tRNA synthetase 2, mitochondrial
summary from NCBI
This gene encodes a putative member of the class II family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of asparagine to tRNA molecules. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency 24 (COXPD24). [provided by RefSeq, Mar 2015]