CDKL5 Proband Entry



Entry ID: cp415

Systematic name: c.65-?_99+?del

Protein name: p.(Ala23Asnfs*3)

Alternate name(s): p.A23fs (deletion of exon 3)

Mutation type: exonic deletion or duplication

Domain: ATP binding region

Pathogenicity class: pathogenic variant

Gender: Male

Phenotype: Not Rett syndrome - early-onset epilepsy

Other mutation:

X-inactivation results: Not applicable

Chromosomal abnormality: Not known

Method of testing: NK, exons 2-21

Source of DNA: blood

Familial testing: de novo

Familial X-inactivation:

Control screening: No

dbSNP ID:

Source: Mirzaa, G.M., Paciorkowski, A.R., Marsh, E.D., Berry-Kravis, E.M., Medne, L., Grix, A., Wirrell, E.C., Powell, B.R., Nickels, K.C., Burton, B., Paras, A., Kim, K., Chung, W., Dobyns, W.B., Das, S. (2013) CDKL5 and ARX mutations in males with early-onset epilepsy. Pediatric Neurology 48:367-377. Pubmed ID: 23583054

Publication ID: 7, LR05-277

Comments:

Entry last updated on: 2014-03-13 06:16:41

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