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Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly v0.27 | TSC1 | Zornitza Stark Marked gene: TSC1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly v0.27 | TSC1 | Zornitza Stark Gene: tsc1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly v0.27 | TSC1 | Zornitza Stark Phenotypes for gene: TSC1 were changed from to Tuberous sclerosis-1, 191100; Autosomal dominant Focal cortical dysplasia, type II, somatic, 607341 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly v0.26 | TSC1 | Zornitza Stark Publications for gene: TSC1 were set to 32917966 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly v0.25 | TSC1 | Zornitza Stark Publications for gene: TSC1 were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly v0.24 | TSC1 | Zornitza Stark Mode of inheritance for gene: TSC1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly v0.23 | TSC1 | Zornitza Stark Tag SV/CNV tag was added to gene: TSC1. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly v0.23 | TSC1 | Elena Savva reviewed gene: TSC1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 32917966; Phenotypes: Tuberous sclerosis-1, 191100, Autosomal dominant Focal cortical dysplasia, type II, somatic, 607341, Lymphangioleiomyomatosis, 606690; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly v0.0 | TSC1 |
Zornitza Stark gene: TSC1 was added gene: TSC1 was added to Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green Mode of inheritance for gene: TSC1 was set to Unknown |