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On this page, you will find information about a genetic change that was identified in an individual. We are trying to find others with the same or similar condition.
A change in the CSNK1G1 gene was identified in an individual with hypotonia, autism, developmental delay, epilepsy, and a feeding tube
Oct 17, 2023
casein kinase 1 gamma
CSNK1G1 is a member of the casein kinase I gene family that is thought to couple Wnt receptor activation to the cytoplasmic signal transduction apparatus (Davidson et al., 2005).
Clinicians and researchers have identified a change in the following gene to be causing the individual’s symptoms:
Interested in learning more about this gene or sharing what you know? Contact us!