MGP Database

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MGP005590

Ontology/Pathway Information

Entrez Gene ID57038
Gene Namearginyl-tRNA synthetase 2, mitochondrial
Gene Symbol RARS2
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005759 TAS:ReactomeCmitochondrial matrix
GO:0005739 IBA:GO_CentralCmitochondrion
GO:0004814 IBA:GO_CentralFarginine-tRNA ligase activity
GO:0005524 IEA:UniProtKB-KWFATP binding
GO:0044822 IDA:UniProtKBFpoly(A) RNA binding
GO:0006420 IBA:GO_CentralParginyl-tRNA aminoacylation
GO:0010467 TAS:ReactomePgene expression
GO:0032543 IBA:GO_CentralPmitochondrial translation
GO:0006418 TAS:ReactomePtRNA aminoacylation for protein translation
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_71Gene Expression
REACT_15302Mitochondrial tRNA aminoacylation
REACT_15482tRNA Aminoacylation
SMP Pathway Links
SMP IDDescription
SMP00020Arginine and Proline Metabolism
SMP00362Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency)
SMP00504Creatine deficiency, guanidinoacetate methyltransferase deficiency
SMP00188Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency)
SMP00506Hyperornithinemia-hyperammonemia-homocitrullinuria [HHH-syndrome]
SMP00505Hyperornithinemia with gyrate atrophy (HOGA)
SMP00361Hyperprolinemia Type I
SMP00360Hyperprolinemia Type II
SMP00507L-arginine:glycine amidinotransferase deficiency
SMP00363Ornithine Aminotransferase Deficiency (OAT Deficiency)
SMP00207Prolidase Deficiency (PD)
SMP00208Prolinemia Type II
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