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The protein encoded by this gene belongs to the prolyl oligopeptidase subfamily of serine peptidases. Mutations in this gene have been associated with hypotonia-cystinuria syndrome, also known as the 2p21 deletion syndrome.
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Protein Aliases: Prolyl endopeptidase-like; Prolylendopeptidase-like; putative prolyl oligopeptidase
Gene Aliases: 2810457N15Rik; 9530014L06Rik; D030028O16Rik; KIAA0436; mKIAA0436; PREPL; RGD1310143
UniProt ID: (Human) Q4J6C6, (Mouse) Q8C167, (Rat) Q5HZA6
Entrez Gene ID: (Human) 9581, (Mouse) 213760, (Rat) 298771
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