Entity Details

Primary name PARS2
Entity type gene
Source Source Link

Details

PrimaryID25973
RefseqGeneNG_042048
SymbolPARS2
Nameprolyl-tRNA synthetase 2, mitochondrial
Chromosome1
Location1p32.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1999-11-21
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSYPM_HUMAN

GO terms

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GOName
GO:0004827 proline-tRNA ligase activity
GO:0005524 ATP binding
GO:0005739 mitochondrion
GO:0005759 mitochondrial matrix
GO:0006433 prolyl-tRNA aminoacylation

Diseases

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Disease IDSourceNameDescription
618437 OMIMDevelopmental and epileptic encephalopathy 75 (DEE75)A form of epileptic encephalopathy, a heterogeneous group of severe early-onset epilepsies characterized by refractory seizures, neurodevelopmental impairment, and poor prognosis. Development is normal prior to seizure onset, after which cognitive and motor delays become apparent. DEE75 is an autosomal recessive form characterized by onset of severe refractory seizures in the first months of life. The disease may be caused by variants affecting the gene represented in this entry.