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Wilms Tumour v0.40 AMER1 Zornitza Stark Marked gene: AMER1 as ready
Wilms Tumour v0.40 AMER1 Zornitza Stark Gene: amer1 has been classified as Red List (Low Evidence).
Wilms Tumour v0.34 AMER1 Chirag Patel changed review comment from: Limited evidence for gene-disease association for Wilms tumour. Four cases of Wilms tumour in unrelated individuals with OSCS.
Sources: Expert list, Expert Review, Literature; to: Limited evidence for presentation with Wilms tumour in disease. Four cases of Wilms tumour in unrelated individuals with OSCS.
Sources: Expert list, Expert Review, Literature
Wilms Tumour v0.34 AMER1 Chirag Patel gene: AMER1 was added
gene: AMER1 was added to Wilms Tumour. Sources: Expert list,Expert Review,Literature
Mode of inheritance for gene: AMER1 was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Publications for gene: AMER1 were set to PMID: 32879452
Phenotypes for gene: AMER1 were set to Wilms tumor, MONDO:0006058; Osteopathia striata with cranial sclerosis, MONDO:0010310; Osteopathia striata with cranial sclerosis. MIM#300373
Review for gene: AMER1 was set to RED
Added comment: Limited evidence for gene-disease association for Wilms tumour. Four cases of Wilms tumour in unrelated individuals with OSCS.
Sources: Expert list, Expert Review, Literature