Activity

Filter

Cancel
Date Panel Item Activity
7 actions
Fetal anomalies v0.4066 TINF2 Zornitza Stark Marked gene: TINF2 as ready
Fetal anomalies v0.4066 TINF2 Zornitza Stark Gene: tinf2 has been classified as Green List (High Evidence).
Fetal anomalies v0.4066 TINF2 Zornitza Stark Phenotypes for gene: TINF2 were changed from EXUDATIVE RETINOPATHY WITH BONE MARROW FAILURE to Revesz syndrome, MIM# 268130
Fetal anomalies v0.4065 TINF2 Zornitza Stark Publications for gene: TINF2 were set to
Fetal anomalies v0.4064 TINF2 Zornitza Stark Mode of inheritance for gene: TINF2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Fetal anomalies v0.4063 TINF2 Zornitza Stark changed review comment from: Bone marrow failure is the main presenting feature. DD is part of the phenotype, neurological involvement progressive.; to: IUGR.
Fetal anomalies v0.0 TINF2 Zornitza Stark gene: TINF2 was added
gene: TINF2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: TINF2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: TINF2 were set to EXUDATIVE RETINOPATHY WITH BONE MARROW FAILURE