CDKL5 Proband Entry

Entry ID: cp413

Systematic name: c.175C>T

Protein name: p.Arg59*

Alternate name(s): p.R59X

Mutation type: nonsense

Domain: catalytic domain

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: direct, exons 2-21

Source of DNA: blood

Familial testing: de novo

Familial X-inactivation:

Control screening: No

dbSNP ID: rs62653623

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: 4, LR03-121


Entry last updated on: 2018-06-05 13:45:42

Similar entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.175C>T p.Arg59* Not Rett syndrome - epileptic encephalopathy Female 16611748 Archer et al (2006) cp48
c.175C>T p.Arg59* Rett syndrome - atypical Female 19740913 Ricciardi et al (2009) cp107
c.175C>T p.Arg59* Rett syndrome - early-onset seizures Female 20493745 Castren et al (2011) cp195
c.175C>T p.Arg59* Rett syndrome - atypical Female 22678952 Bahi-Buisson et al (2012) cp456

Displaying a total number of 4 proband entries.