HINT1 Pathway (Homo sapiens)

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<?xml version="1.0" encoding="UTF-8"?> <Pathway xmlns="http://pathvisio.org/GPML/2013a" Name="HINT1 Pathway" Version="20250217" Organism="Homo sapiens"> <Comment Source="WikiPathways-description">HINT1 is a protein that can be mutated in charcot marie tooth disease.</Comment> <Graphics BoardWidth="1203.0" BoardHeight="931.8303333136264" /> <DataNode TextLabel="cyclin H" GraphId="ad8f6" Type="GeneProduct" GroupRef="f5a5c"> <Graphics CenterX="104.87528344671287" CenterY="130.61224489795998" Width="90.0" Height="38.09523809523809" ZOrder="32768" FontSize="12" Valign="Middle" /> <Xref Database="Uniprot-TrEMBL" ID="P51946" /> </DataNode> <DataNode TextLabel="AP1 complex" GraphId="b2810" Type="Complex" GroupRef="cb2f3"> <Graphics CenterX="604.8000000000044" CenterY="65.10000000000046" Width="90.0" Height="25.0" ZOrder="32768" FontSize="12" Valign="Middle" /> <Xref Database="" ID="CPX-480" /> </DataNode> <DataNode TextLabel="TCF4" GraphId="e8e52" Type="GeneProduct" GroupRef="d52bd"> <Graphics 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