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Fetal anomalies v0.2658 FMN2 Zornitza Stark Marked gene: FMN2 as ready
Fetal anomalies v0.2658 FMN2 Zornitza Stark Gene: fmn2 has been classified as Red List (Low Evidence).
Fetal anomalies v0.2658 FMN2 Zornitza Stark Phenotypes for gene: FMN2 were changed from NONSYNDROMIC AUTOSOMAL-RECESSIVE INTELLECTUAL DISABILITY to Intellectual developmental disorder, autosomal recessive 47, MIM#616193
Fetal anomalies v0.2657 FMN2 Zornitza Stark Publications for gene: FMN2 were set to
Fetal anomalies v0.2656 FMN2 Zornitza Stark Classified gene: FMN2 as Red List (low evidence)
Fetal anomalies v0.2656 FMN2 Zornitza Stark Gene: fmn2 has been classified as Red List (Low Evidence).
Fetal anomalies v0.2366 FMN2 Belinda Chong reviewed gene: FMN2: Rating: RED; Mode of pathogenicity: None; Publications: 25480035, 32162566, 24161494; Phenotypes: Intellectual developmental disorder, autosomal recessive 47 MIM#616193; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Fetal anomalies v0.0 FMN2 Zornitza Stark gene: FMN2 was added
gene: FMN2 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: FMN2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: FMN2 were set to NONSYNDROMIC AUTOSOMAL-RECESSIVE INTELLECTUAL DISABILITY