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PTRH1 (Peptidyl-TRNA Hydrolase 1 Homolog) is a Protein Coding gene. Diseases associated with PTRH1 include Vascular Skin Disease and Early Infantile Epileptic Encephalopathy. Gene Ontology (GO) annotations related to this gene include aminoacyl-tRNA hydrolase activity.
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Protein Aliases: Peptidyl-tRNA hydrolase; Probable peptidyl-tRNA hydrolase; PTH
Gene Aliases: 2210013M04Rik; AW046744; C9orf115; PTH1; PTRH1; RGD1310165
UniProt ID: (Human) Q86Y79, (Mouse) Q8BW00
Entrez Gene ID: (Human) 138428, (Rat) 362113, (Mouse) 329384
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