Variant information


Systematic Name
(NM_004992.3:)		 c.1044-?_1442+?del
Protein name
(NP_004983)		 p.?
Alternate systematic Name
(NM_001110792.1:)		 c.1080_1478del
Alternate Protein name
(NP_001104262)		 p.(Ser361_Val493del)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153295837_153296235del
Mutation type exonic deletions
Domain C-term
Pathogenicity Mutation associated with disease

View proband information


No: Systematic Name Protein name Gender Phenotype Proband id References View
1 c.1044-?_1442+?del p.? Female Rett syndrome-atypical 5138 MECP2 gene study in a large cohort testing of 240 female patients and 861 healthy controls (519 females and 342 males):Maortua, H., Martinez-Bouzas, C., Garcia-Ribes, A., Martinez, M.-J., Guillen, E., Domingo, M.-R., Calvo, M.-T., Guitart, M., Gabau, E., Botella, M.-P., Gener, B., Rubio, I., Lopez-Ariztegui, M.-A., Tejada, M.-I.:J Mol Diagn: 23810759 View details
2 c.1044-?_1442+?del p.? Female Rett syndrome-atypical 5139 MECP2 gene study in a large cohort testing of 240 female patients and 861 healthy controls (519 females and 342 males):Maortua, H., Martinez-Bouzas, C., Garcia-Ribes, A., Martinez, M.-J., Guillen, E., Domingo, M.-R., Calvo, M.-T., Guitart, M., Gabau, E., Botella, M.-P., Gener, B., Rubio, I., Lopez-Ariztegui, M.-A., Tejada, M.-I.:J Mol Diagn: 23810759 View details