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

Date of Report

Oct 17, 2023

Full Name

casein kinase 1 gamma

Chromosome 15 (15q22.31)


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).

Database Links

GeneCards: CSNK1G1

NCBI Gene: 53944

OMIM: 606274

UniProtKB/Swiss-Prot: Q9HCP0

Clinical Significance

Clinicians and researchers have identified a change in the following gene to be causing the individual’s symptoms:

Gene CSNK1G1
Inheritance Pattern Unknown
Position (hg19) Unknown
Transcript Unknown
DNA Change Unknown
Protein Change Unknown
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