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Severe Paediatric Disorders v0.12 TMEM5 Louise Daugherty edited their review of gene: TMEM5: Added comment: Initial gene list (NGC_genelist-20190823_GREEN_dis_moi_forCuration_20200211.xlsx) collated by Dr Courtney French (University of Cambridge University Hospital NHS Foundation), Dr Karyn Megy (Clinical Feedback Lead, NIHR BioResource - Rare Diseases Study, University of Cambridge University Hospital NHS Foundation), Dr Alba Sanchis-Juan (NIHR BioResource - Rare Diseases Study, University of Cambridge University Hospital NHS Foundation) and Lucy Raymond (Professor of Medical Genetics and Neurodevelopment, University of Cambridge University Hospital NHS Foundation). Submitted to the PanelApp resource January 2020 on behalf of the Next Generation Children Project, Addenbrookes' Hospital, Cambridge. Gene Symbol submitted: TMEM5; Recommended initial gene rating: Green List (high evidence); Phenotypes: Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, 615041 (3); Mode of inheritance: Autosomal recessive; Changed rating: AMBER
Severe Paediatric Disorders v0.11 TMEM5 Louise Daugherty Publications for gene TMEM5 were updated from to 30847515
Severe Paediatric Disorders v0.10 TMEM5 Louise Daugherty Added phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, 615041 for gene: TMEM5
Severe Paediatric Disorders v0.9 TMEM5 Louise Daugherty Added phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, 615041 for gene: TMEM5
Severe Paediatric Disorders v0.9 TMEM5 Louise Daugherty Added phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, 615041 for gene: TMEM5
Severe Paediatric Disorders v0.8 TMEM5 Louise Daugherty Added phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, 615041 for gene: TMEM5
Severe Paediatric Disorders v0.8 TMEM5 Louise Daugherty Mode of inheritance for gene TMEM5 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10, 615041 for gene: TMEM5
Severe Paediatric Disorders v0.7 TMEM5 Louise Daugherty commented on gene: TMEM5
Severe Paediatric Disorders v0.7 TMEM5 Louise Daugherty Source Next Generation Children Project was added to TMEM5.
Severe Paediatric Disorders v0.6 TMEM5 Louise Daugherty Tag new-gene-name tag was added to gene: TMEM5.
Severe Paediatric Disorders v0.5 TMEM5 Louise Daugherty Source Expert Review Green was added to TMEM5.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 TMEM5 Louise Daugherty gene: TMEM5 was added
gene: TMEM5 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: TMEM5 was set to