CCDC53
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<h1>ccdc53: An In-Depth Look</h1>
<h2>Description</h2>
<p>ccdc53 is a gene that encodes a protein called coiled-coil domain containing 53. This protein is involved in a variety of cellular processes, including cell growth, differentiation, and apoptosis. Mutations in the ccdc53 gene have been linked to a number of diseases, including:</p>
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<li>Congenital heart defects</li>
<li>Intellectual disability</li>
<li>Autism spectrum disorder</li>
<li>Schizophrenia</li>
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<h2>Associated Diseases</h2>
<p>ccdc53 mutations have been associated with a number of diseases, including:</p>
<ul>
<li>Congenital heart defects: Mutations in the ccdc53 gene have been linked to a number of congenital heart defects, including atrial septal defect, ventricular septal defect, and tetralogy of Fallot.</li>
<li>Intellectual disability: Mutations in the ccdc53 gene have been linked to intellectual disability, a condition characterized by significant limitations in intellectual functioning.</li>
<li>Autism spectrum disorder: Mutations in the ccdc53 gene have been linked to autism spectrum disorder, a developmental disorder characterized by social and communication difficulties.</li>
<li>Schizophrenia: Mutations in the ccdc53 gene have been linked to schizophrenia, a mental disorder characterized by hallucinations, delusions, and disorganized thinking.</li>
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**Did you Know ?**
<p>Approximately 1 in 100,000 people are born with a mutation in the ccdc53 gene.</p>
