CDH8: Difference between revisions
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Latest revision as of 05:53, 17 March 2025
CDH8 or Cadherin 8 is a protein that in humans is encoded by the CDH8 gene. Cadherins are calcium-dependent cell-cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. CDH8 is thought to play an important role in brain development and function.
Function[edit]
CDH8 is a type II classical cadherin from the cadherin superfamily. The encoded protein is a calcium-dependent cell-cell adhesion glycoprotein composed of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. Type II (atypical) cadherins are defined based on their lack of a HAV cell adhesion recognition sequence specific to type I cadherins. This particular cadherin is expressed in brain and is putatively involved in synaptic adhesion, axon outgrowth and guidance.
Clinical significance[edit]
Mutations in the CDH8 gene have been associated with Autism Spectrum Disorder (ASD). A study published in 2014 found that rare, probably gene-disrupting (pD) variation in CDH8 is associated with a high risk for ASD. The study also found that the CDH8 gene is expressed in the developing human brain, particularly in regions involved in language and cognition.
See also[edit]
References[edit]
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