CDKL5
cyclin dependent kinase like 5
Normal Function
Health Conditions Related to Genetic Changes
CDKL5 deficiency disorder
At least 150 mutations in the CDKL5 gene have been found to cause CDKL5 deficiency disorder. This rare condition is characterized by seizures that begin in infancy, followed by significant delays in many aspects of development. Affected individuals have severe intellectual disability and most do not walk independently. About 90 percent of people diagnosed with CDKL5 deficiency disorder are female.
CDKL5 deficiency disorder was previously classified as an atypical form of Rett syndrome. However, CDKL5 deficiency disorder is now considered a separate condition. Rett syndrome, which affects development in girls and women, results from mutations in the MECP2 gene. Because the CDKL5 and MeCP2 proteins may interact in the brain, the two disorders might be caused by a similar mechanism.
Mutations in the CDKL5 gene reduce the amount of functional CDKL5 protein or alter its activity in neurons. A shortage (deficiency) of CDKL5 or impairment of its function disrupts brain development, but it is unclear how these changes cause the specific features of CDKL5 deficiency disorder.
Most CDKL5 gene mutations change single protein building blocks (amino acids) in the CDKL5 protein. This type of mutation occurs most often in a region of the protein called the kinase domain, which is essential for the protein's kinase function. Mutations in the kinase domain disrupt the ability of CDKL5 to add phosphate groups to other proteins. Compared with other types of mutation, these mutations are associated with more severe signs and symptoms of CDKL5 deficiency disorder.
Other CDKL5 gene mutations alter different regions of the CDKL5 protein or lead to the production of an abnormally short version of the protein. Research has shown that mutations affecting parts of the protein other than the kinase domain tend to cause less severe signs and symptoms of CDKL5 deficiency disorder than other types of mutations.
More About This Health ConditionRelated Conditions
CDKL5 deficiency disorder
Health Conditions Related to Genetic Changes
At least 150 mutations in the CDKL5 gene have been found to cause CDKL5 deficiency disorder. This rare condition is characterized by seizures that begin in infancy, followed by significant delays in many aspects of development. Affected individuals have severe intellectual disability and most do not walk independently. About 90 percent of people diagnosed with CDKL5 deficiency disorder are female.
CDKL5 deficiency disorder was previously classified as an atypical form of Rett syndrome. However, CDKL5 deficiency disorder is now considered a separate condition. Rett syndrome, which affects development in girls and women, results from mutations in the MECP2 gene. Because the CDKL5 and MeCP2 proteins may interact in the brain, the two disorders might be caused by a similar mechanism.
Mutations in the CDKL5 gene reduce the amount of functional CDKL5 protein or alter its activity in neurons. A shortage (deficiency) of CDKL5 or impairment of its function disrupts brain development, but it is unclear how these changes cause the specific features of CDKL5 deficiency disorder.
Most CDKL5 gene mutations change single protein building blocks (amino acids) in the CDKL5 protein. This type of mutation occurs most often in a region of the protein called the kinase domain, which is essential for the protein's kinase function. Mutations in the kinase domain disrupt the ability of CDKL5 to add phosphate groups to other proteins. Compared with other types of mutation, these mutations are associated with more severe signs and symptoms of CDKL5 deficiency disorder.
Other CDKL5 gene mutations alter different regions of the CDKL5 protein or lead to the production of an abnormally short version of the protein. Research has shown that mutations affecting parts of the protein other than the kinase domain tend to cause less severe signs and symptoms of CDKL5 deficiency disorder than other types of mutations.