DYX1C1

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Template:Short description Template:Infobox gene Dyslexia susceptibility 1 candidate gene 1 protein is a protein that in humans is encoded by the DYX1C1 gene.[1][2] This protein contains 420 amino acids with 3 tetratricopeptide repeat (TPR) domains, thought to mediate protein–protein interactions.

Clinical significance

A mutation in the DYX1C1 gene has been associated with deficits in reading ability (dyslexia).[1][3]

References

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Further reading

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