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Arthrogryposis v3.154 MYL1 Ivone Leong Tag Q2_21_rating was removed from gene: MYL1.
Arthrogryposis v3.154 MYL1 Sarah Leigh commented on gene: MYL1
Arthrogryposis v3.153 MYL1 Ivone Leong Source Expert Review Red was added to MYL1.
Rating Changed from Green List (high evidence) to Red List (low evidence)
Arthrogryposis v3.66 MYL1 Arina Puzriakova Publications for gene: MYL1 were set to
Arthrogryposis v3.65 MYL1 Arina Puzriakova Classified gene: MYL1 as Green List (high evidence)
Arthrogryposis v3.65 MYL1 Arina Puzriakova Added comment: Comment on list classification: Only mild contractures described in 1/2 individuals with variants in this gene. Therefore, there is only enough evidence for a RED rating on this panel at present. These cases would still expected to be picked up via the 'Congenital myopathy' or 'Fetal anomalies' routes for which this gene is Green.
Arthrogryposis v3.65 MYL1 Arina Puzriakova Gene: myl1 has been classified as Green List (High Evidence).
Arthrogryposis v3.64 MYL1 Arina Puzriakova Tag Q2_21_rating tag was added to gene: MYL1.
Arthrogryposis v3.64 MYL1 Arina Puzriakova commented on gene: MYL1
Arthrogryposis v3.62 MYL1 Arina Puzriakova Phenotypes for gene: MYL1 were changed from congenital myopathy to Myopathy, congenital, with fast-twitch (type II) fiber atrophy, OMIM:618414; Congenital myopathy with reduced type 2 muscle fibers, MONDO:0034109
Arthrogryposis v3.11 MYL1 Zornitza Stark reviewed gene: MYL1: Rating: RED; Mode of pathogenicity: None; Publications: 30215711; Phenotypes: Myopathy, congenital, with fast-twitch (type II) fiber atrophy, MIM# 618414; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Arthrogryposis v2.64 MYL1 Rebecca Foulger reviewed gene: MYL1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Arthrogryposis v2.63 MYL1 Rebecca Foulger gene: MYL1 was added
gene: MYL1 was added to Arthrogryposis. Sources: Other,Expert Review Green
Mode of inheritance for gene: MYL1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: MYL1 were set to congenital myopathy