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Fetal anomalies v0.2632 MYO18B Zornitza Stark Marked gene: MYO18B as ready
Fetal anomalies v0.2632 MYO18B Zornitza Stark Gene: myo18b has been classified as Green List (High Evidence).
Fetal anomalies v0.2632 MYO18B Zornitza Stark Publications for gene: MYO18B were set to 27858739; 25748484; 27879346
Fetal anomalies v0.2631 MYO18B Zornitza Stark Classified gene: MYO18B as Green List (high evidence)
Fetal anomalies v0.2631 MYO18B Zornitza Stark Gene: myo18b has been classified as Green List (High Evidence).
Fetal anomalies v0.2352 MYO18B Ain Roesley reviewed gene: MYO18B: Rating: GREEN; Mode of pathogenicity: None; Publications: 25748484, 27858739, 32637634, 32184166, 27879346, 33179433; Phenotypes: Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism MIM#616549; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Fetal anomalies v0.0 MYO18B Zornitza Stark gene: MYO18B was added
gene: MYO18B was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: MYO18B was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MYO18B were set to 27858739; 25748484; 27879346
Phenotypes for gene: MYO18B were set to Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome, MONDO:0014689; Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism, OMIM:616549