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
Comments:
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.