FOXG1 Proband Entry



   CSV explantation textc


Entry ID: fp20

Systematic name: c.256C>T

Protein name: p.Gln86*

Alternate name(s):

Mutation type: nonsense

Domain: Inter domain region

Pathogenicity class: pathogenic variant

Gender: Female

Phenotype: Rett syndrome - sporadic

Other mutation: NK

Chromosomal abnormality: Not known

Method of testing: direct, MECP2 negative

Source of DNA: blood

Familial testing: not in mother

Control screening: No

dbSNP ID:

Source: Kortum, F., Das, S., Flindt, M., Morris-Rosendahl, J., Stefanova, I., Goldstein, A., Horn, D., Klopocki, E., Kluger, G., Martin, P., Rauch, A., Roumer, A., Saitta, S., Walsh, L.E., Wieczorek, D., Uyanik, G., Kutsche, K., Dobyns, W.B. (2011) The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. Journal of Medical Genetics 48:396-406. Pubmed ID: 21441262

Publication ID: 9

Comments:

Entry last updated on: 2015-12-02 01:18:46

Similar entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.256C>T p.Gln86* Not Rett syndrome - sporadic Female 24836831 Seltzer, L.E. et al (2014) fp40

Displaying a total number of 1 proband entries.