CDKL5 Proband Entry
Entry ID: cp303
Systematic name: c.1455_1460delGGCCAA
Protein name: p.Ala486_Lys487del
Alternate name(s): p.A486_K487del
Mutation type: in-frame insertion and/or deletion
Domain: not specified
Pathogenicity class: likely benign variant
Gender: Female
Phenotype: Not known - unaffected family member
Other mutation:
X-inactivation results: Yes - random
Chromosomal abnormality: Not known
Method of testing: CSGE, MECP2 negative
Source of DNA: not certain
Familial testing: No
Familial X-inactivation:
Control screening: not found in 200/200 chromosomes
dbSNP ID:
Source: Maortua, H., Martinez-Bouzas, C., Calvo, M.-T., Domingo, M.-R., Ramos, F., Garcia-Ribes, A., Martinez, M.-J., Lopez-Ariztegui, M.-A., Puente, N., Rubio, I., Tejada, M.-I. (2012) CDKL5 gene status in female patients with epilepsy and Rett-like features: two new mutations in the catalytic domain. BMC Medical Genetics 13:68. Pubmed ID: 22867051
Publication ID:
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.1455_1460delGGCCAA | p.Ala486_Lys487del | Not Rett syndrome - infantile-onset seizures | Female | 22867051 Maortua et al (2012) | cp302 |
Displaying a total number of 1 proband entries.