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<a accesskey="3" href="page.php?w=GTF2I&amp;p=2">3.Next</a>
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<p><b>General transcription factor II-I</b> is a <a href="page.php?w=protein">protein</a> that in humans is encoded by the GTF2I <a href="page.php?w=gene">gene</a>.</p>

<p><big> Function </big></p>
<p>This gene encodes a multifunctional phosphoprotein, TFII-I, with roles in transcription and signal transduction. Haploinsuffiency (deletion of one copy) of the GTF2I gene is noted in <a href="page.php?w=Williams-Beuren_syndrome">Williams-Beuren syndrome</a>, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23.</p><p>
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