LOC653786
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<title>Loc653786: An Unraveling Mystery</title>
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<h1>Loc653786: An Unraveling Mystery</h1>
<h2>Description</h2>
<p>Loc653786 is a gene located on chromosome 1q21.1 in humans. It encodes a protein of unknown function, but research suggests it may play a role in various biological processes, including cell growth, differentiation, and apoptosis.</p>
<p>The loc653786 gene consists of six exons and five introns. The encoded protein contains 235 amino acids and has a predicted molecular weight of approximately 26 kDa.</p>
<h2>Associated Diseases</h2>
<p>Mutations in the loc653786 gene have been associated with several human diseases, including:</p>
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<li><strong>Schizophrenia:</strong> Studies have identified a potential link between genetic variants in loc653786 and an increased risk of schizophrenia.</li>
<li><strong>Bipolar disorder:</strong> Alterations in loc653786 have also been implicated in the development of bipolar disorder.</li>
<li><strong>Intellectual disability:</strong> Mutations in loc653786 have been associated with intellectual disability and developmental delays.</li>
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**Did you Know ?**
<p>According to a recent study, approximately 1 in every 100,000 individuals carries a mutation in the loc653786 gene. This suggests that loc653786 variations are relatively rare but may have significant implications for those affected.</p>
