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Overview
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Calculated MW: 84 kDa
Observed MW: Refer to figures
Gene Accession: BC013193Please contact us at for specific academic pricing.
Background
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. Several alternatively spliced transcript variants encoding either the same or different isoforms have been described for this gene.
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