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Fetal anomalies v0.3446 TMEM126B Zornitza Stark Marked gene: TMEM126B as ready
Fetal anomalies v0.3446 TMEM126B Zornitza Stark Gene: tmem126b has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.3446 TMEM126B Zornitza Stark Phenotypes for gene: TMEM126B were changed from Muscle Weakness and Isolated Complex I Deficiency to Mitochondrial complex I deficiency, nuclear type 29 (MIM#618250)
Fetal anomalies v0.3445 TMEM126B Zornitza Stark Publications for gene: TMEM126B were set to
Fetal anomalies v0.3444 TMEM126B Zornitza Stark Classified gene: TMEM126B as Amber List (moderate evidence)
Fetal anomalies v0.3444 TMEM126B Zornitza Stark Gene: tmem126b has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.3396 TMEM126B Daniel Flanagan reviewed gene: TMEM126B: Rating: AMBER; Mode of pathogenicity: None; Publications: 27374774, 27374773; Phenotypes: Mitochondrial complex I deficiency, nuclear type 29 (MIM#618250); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal anomalies v0.0 TMEM126B Zornitza Stark gene: TMEM126B was added
gene: TMEM126B was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: TMEM126B was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: TMEM126B were set to Muscle Weakness and Isolated Complex I Deficiency