CDKL5 Proband Entry
Entry ID: cp51
Systematic name: c.978-49_978-41del9
Protein name: p.?
Alternate name(s): intronic variation (IVS11-49_-41del9)
Mutation type: intronic variant
Domain: not specified
Pathogenicity class: likely benign variant
Gender: Female
Phenotype: Not Rett syndrome - not certain
Other mutation:
X-inactivation results: Yes - random
Chromosomal abnormality: Not known
Method of testing: DHPLC, exons 2-21
Source of DNA: lymphocyte
Familial testing: No
Familial X-inactivation:
Control screening: No
dbSNP ID: rs267608554
Source: Archer, H.L., Evans, J., Edwards, S., Colley, J., Newbury-Ecob, R., O'Callaghan, F., Huyton, M., O'Regan, M., Tolmie, J., Sampson, J., Clarke, A., Osborne, J. (2006) CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients. J Med Genet 43:729-734. Pubmed ID: 16611748
Publication ID: patient 8
Comments:
Entry last updated on: 2018-06-05 13:45:42
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There are no other entries in the database with a similar genotype.