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Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.108 TPM3 Ellen McDonagh changed review comment from: Comment on list classification: Gene to be kept Red until further evidence for this to be appropriate on this panel.; to: Comment on list classification: This gene will remain Red based on the review and comments from Chiara Marini Bettolo (NUTH).
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.104 TPM3 Ellen McDonagh Classified gene: TPM3 as Red List (low evidence)
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.104 TPM3 Ellen McDonagh Added comment: Comment on list classification: Gene to be kept Red until further evidence for this to be appropriate on this panel.
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.104 TPM3 Ellen McDonagh Gene: tpm3 has been classified as Red List (Low Evidence).
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.97 TPM3 Chiara Marini Bettolo edited their review of gene: TPM3: Added comment: CAP myopathy, nemaline myopathy, congenital myopathy with fibre type disproportion; Changed rating: RED
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.86 TPM3 Louise Daugherty Source NHS GMS was added to TPM3.
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.85 TPM3 Louise Daugherty Source Yorkshire and North East GLH was added to TPM3.
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.50 TPM3 Louise Daugherty Phenotypes for gene: TPM3 were changed from CAP myopathy 1, 609284; Nemaline myopathy 1, autosomal dominant or recessive, 609284 to CAP myopathy 1, 609284; Nemaline myopathy 1, autosomal dominant or recessive, 609284; Nemaline myopathy; congenital myopathy
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.46 TPM3 Chiara Marini Bettolo reviewed gene: TPM3: Rating: GREEN; Mode of pathogenicity: None; Publications: 7704029, 10619715; Phenotypes: Nemaline myopathy, congenital myopathy; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.18 TPM3 Louise Daugherty Mode of inheritance for gene TPM3 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes CAP myopathy 1, 609284; Nemaline myopathy 1, autosomal dominant or recessive, 609284 for gene: TPM3
Publications for gene TPM3 were changed from to 7704029; 10619715
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.17 TPM3 Ana Topf reviewed gene: TPM3: Rating: GREEN; Mode of pathogenicity: ; Publications: 7704029, 10619715; Phenotypes: Nemaline myopathy 1, autosomal dominant or recessive, 609284, CAP myopathy 1, 609284; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies v1.16 TPM3 Louise Daugherty gene: TPM3 was added
gene: TPM3 was added to Limb girdle muscular dystrophy. Sources: Expert Review
Mode of inheritance for gene: TPM3 was set to