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Epidermolysis bullosa v2.0 DSG1 Gene migrated from ENSG00000134760 to ENSG00000134760 (gene set migration)
Epidermolysis bullosa v1.3 DSG1 Zornitza Stark Publications for gene: DSG1 were set to 19558595; 23974871; 29229434
Epidermolysis bullosa v1.3 DSG1 Zornitza Stark Publications for gene: DSG1 were set to 19558595; 23974871
Epidermolysis bullosa v1.2 DSG1 Zornitza Stark Classified gene: DSG1 as Green List (high evidence)
Epidermolysis bullosa v1.2 DSG1 Zornitza Stark Gene: dsg1 has been classified as Green List (High Evidence).
Epidermolysis bullosa v1.1 DSG1 Chern Lim reviewed gene: DSG1: Rating: GREEN; Mode of pathogenicity: None; Publications: 29229434; Phenotypes: ; Mode of inheritance: None; Current diagnostic: yes
Epidermolysis bullosa v0.35 DSG1 Zornitza Stark Marked gene: DSG1 as ready
Epidermolysis bullosa v0.35 DSG1 Zornitza Stark Gene: dsg1 has been classified as Amber List (Moderate Evidence).
Epidermolysis bullosa v0.35 DSG1 Zornitza Stark Classified gene: DSG1 as Amber List (moderate evidence)
Epidermolysis bullosa v0.35 DSG1 Zornitza Stark Gene: dsg1 has been classified as Amber List (Moderate Evidence).
Epidermolysis bullosa v0.24 DSG1 Ain Roesley gene: DSG1 was added
gene: DSG1 was added to Epidermolysis bullosa. Sources: Literature
Mode of inheritance for gene: DSG1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: DSG1 were set to 19558595; 23974871
Phenotypes for gene: DSG1 were set to Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE, AR (MIM#615508); Keratosis palmoplantaris striata I, AD (MIM# 148700)
Penetrance for gene: DSG1 were set to unknown
Review for gene: DSG1 was set to AMBER
Added comment: skin blistering and/or fragility reported in 2 probands

PMID: 19558595;
- 40-yr old man presented with painful thickening of the skin on his palms and soles, hyperhidrosis and intermittent associated blistering, since childhood
- heterozygous p.(Arg144*)

PMID: 23974871;
(authors are calling it SAM syndrome)
- 2 families in this report with 1 individual presenting with skin erosions and scaling homozygous for c.49–1G>A
Sources: Literature