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Fetal anomalies v1.976 TGFB1 Arina Puzriakova Phenotypes for gene: TGFB1 were changed from CAMURATI-ENGELMANN DISEASE to Camurati-Engelmann disease, OMIM:131300
Fetal anomalies v0.337 TGFB1 Rebecca Foulger edited their review of gene: TGFB1: Changed rating: RED
Fetal anomalies v0.319 TGFB1 Rebecca Foulger Classified gene: TGFB1 as Red List (low evidence)
Fetal anomalies v0.319 TGFB1 Rebecca Foulger Gene: tgfb1 has been classified as Red List (Low Evidence).
Fetal anomalies v0.318 TGFB1 Rebecca Foulger commented on gene: TGFB1: This gene was reviewed by Anna de Burca (Genomics England clinical team) and Melita Irving. Melita said seemed unlikely to present in a fetus so demoted rating from Green to Red.
Fetal anomalies v0.9 TGFB1 Rebecca Foulger commented on gene: TGFB1: DDG2P rating in original PAGE list: Confirmed for CAMURATI-ENGELMANN DISEASE
Fetal anomalies v0.3 TGFB1 Rebecca Foulger reviewed gene: TGFB1: Rating: AMBER; Mode of pathogenicity: Other - please provide details in the comments; Publications: ; Phenotypes: ; Mode of inheritance:
Fetal anomalies v0.1 TGFB1 Rebecca Foulger gene: TGFB1 was added
gene: TGFB1 was added to Fetal anomalies. Sources: Expert Review Green,PAGE DD-Gene2Phenotype
Mode of inheritance for gene: TGFB1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: TGFB1 were set to CAMURATI-ENGELMANN DISEASE