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Fetal anomalies v0.2574 EXPH5 Zornitza Stark Marked gene: EXPH5 as ready
Fetal anomalies v0.2574 EXPH5 Zornitza Stark Gene: exph5 has been classified as Red List (Low Evidence).
Fetal anomalies v0.2574 EXPH5 Zornitza Stark Phenotypes for gene: EXPH5 were changed from INHERITED SKIN FRAGILITY to Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive, OMIM #615028
Fetal anomalies v0.2573 EXPH5 Zornitza Stark Publications for gene: EXPH5 were set to
Fetal anomalies v0.2572 EXPH5 Zornitza Stark Classified gene: EXPH5 as Red List (low evidence)
Fetal anomalies v0.2572 EXPH5 Zornitza Stark Gene: exph5 has been classified as Red List (Low Evidence).
Fetal anomalies v0.2571 EXPH5 Zornitza Stark reviewed gene: EXPH5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Fetal anomalies v0.2206 EXPH5 Chirag Patel Classified gene: EXPH5 as Green List (high evidence)
Fetal anomalies v0.2206 EXPH5 Chirag Patel Gene: exph5 has been classified as Green List (High Evidence).
Fetal anomalies v0.2205 EXPH5 Chirag Patel reviewed gene: EXPH5: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 23176819, 32176379, 26211931, 27384765, 27730671; Phenotypes: Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive, OMIM #615028; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal anomalies v0.0 EXPH5 Zornitza Stark gene: EXPH5 was added
gene: EXPH5 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: EXPH5 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: EXPH5 were set to INHERITED SKIN FRAGILITY