CDKL5 Variant



Variant ID: cm141

Systematic name: c.2377-?_*1085del

Protein name: p.?

Alternate name(s): p.? (deletion of exons 17 to 21)

Mutation type: exonic deletion or duplication

Domain: regulatory C-terminal

Pathogenicity class: pathogenic variant

dbSNP ID:

First reference: Liang, J.-S., Shimojima, K., Takayama, R., Natsume, J., Shichiji, M., Hirasawa, K., Kimai, K., Okanishi, T., Mizuno, S., Okumura, A., Sugawara, M., Ito, T., Ikeda, H., Takahashi, Y., Oguni, H., Imai, K., Osawa, M., Yamamoto, T. (2011) CDKL5 alterations lead to early epileptic encephalopathy in both genders. Epilepsia 52:1835-1842. Pubmed ID: 21770923

Comments:

Variant last updated on: 2014-03-13 05:51:47

Matching entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.2377-?_*1085del p.? Not Rett syndrome - epileptic encephalopathy Female 21770923, Liang et al (2011) cp298

Displaying a total number of 1 proband entries matching this variant.