CDKL5 Proband Entry



Entry ID: cp298

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

Gender: Female

Phenotype: Not Rett syndrome - epileptic encephalopathy

Other mutation:

X-inactivation results: No

Chromosomal abnormality: Yes - deletion involving CDKL5 (after exon 16) and RS1

Method of testing: array CGH

Source of DNA: blood

Familial testing: de novo

Familial X-inactivation:

Control screening: No

dbSNP ID:

Source: 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

Publication ID: 4

Comments:

Entry last updated on: 2014-03-13 06:13:10

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