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Pulmonary Fibrosis_Interstitial Lung Disease v0.80 WFDC2 Zornitza Stark Phenotypes for gene: WFDC2 were changed from bronchiectasis, MONDO:0004822, WFDC2-related to Bronchiectasis and nasal polyposis, MIM# 620984
Pulmonary Fibrosis_Interstitial Lung Disease v0.79 WFDC2 Zornitza Stark edited their review of gene: WFDC2: Changed phenotypes: Bronchiectasis and nasal polyposis, MIM# 620984
Pulmonary Fibrosis_Interstitial Lung Disease v0.79 WFDC2 Zornitza Stark Marked gene: WFDC2 as ready
Pulmonary Fibrosis_Interstitial Lung Disease v0.79 WFDC2 Zornitza Stark Gene: wfdc2 has been classified as Green List (High Evidence).
Pulmonary Fibrosis_Interstitial Lung Disease v0.79 WFDC2 Zornitza Stark Tag founder tag was added to gene: WFDC2.
Pulmonary Fibrosis_Interstitial Lung Disease v0.79 WFDC2 Zornitza Stark Classified gene: WFDC2 as Green List (high evidence)
Pulmonary Fibrosis_Interstitial Lung Disease v0.79 WFDC2 Zornitza Stark Gene: wfdc2 has been classified as Green List (High Evidence).
Pulmonary Fibrosis_Interstitial Lung Disease v0.78 WFDC2 Zornitza Stark gene: WFDC2 was added
gene: WFDC2 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Literature
Mode of inheritance for gene: WFDC2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: WFDC2 were set to 38626355
Phenotypes for gene: WFDC2 were set to bronchiectasis, MONDO:0004822, WFDC2-related
Review for gene: WFDC2 was set to GREEN
Added comment: 11 individuals from 10 families reported with bi-allelic variants in this gene and bronchiectasis and nasal polyps. p.Cys49Arg is recurrent and may be a founder variant.
Sources: Literature