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: 2018-06-05 13:45:42
Similar entries in the proband database
There are no other entries in the database with a similar genotype.