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Susceptibility to Viral Infections v0.93 MCM10 Zornitza Stark Publications for gene: MCM10 were set to 32865517
Susceptibility to Viral Infections v0.92 MCM10 Zornitza Stark Classified gene: MCM10 as Amber List (moderate evidence)
Susceptibility to Viral Infections v0.92 MCM10 Zornitza Stark Gene: mcm10 has been classified as Amber List (Moderate Evidence).
Susceptibility to Viral Infections v0.91 MCM10 Peter McNaughton reviewed gene: MCM10: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 33712616; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Susceptibility to Viral Infections v0.75 MCM10 Zornitza Stark Phenotypes for gene: MCM10 were changed from Susceptibility to CMV to Immunodeficiency-80 with or without congenital cardiomyopathy (IMD80), MIM#619313; Susceptibility to CMV
Susceptibility to Viral Infections v0.74 MCM10 Zornitza Stark edited their review of gene: MCM10: Changed phenotypes: Immunodeficiency-80 with or without congenital cardiomyopathy (IMD80), MIM#619313, Susceptibility to CMV
Susceptibility to Viral Infections v0.72 MCM10 Zornitza Stark edited their review of gene: MCM10: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Susceptibility to Viral Infections v0.67 MCM10 Zornitza Stark Marked gene: MCM10 as ready
Susceptibility to Viral Infections v0.67 MCM10 Zornitza Stark Gene: mcm10 has been classified as Red List (Low Evidence).
Susceptibility to Viral Infections v0.67 MCM10 Zornitza Stark Mode of inheritance for gene: MCM10 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BIALLELIC, autosomal or pseudoautosomal
Susceptibility to Viral Infections v0.66 MCM10 Zornitza Stark gene: MCM10 was added
gene: MCM10 was added to Susceptibility to Viral Infections. Sources: Literature
Mode of inheritance for gene: MCM10 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MCM10 were set to 32865517
Phenotypes for gene: MCM10 were set to Susceptibility to CMV
Review for gene: MCM10 was set to RED
Added comment: Compound heterozygous variants in minichromosomal maintenance complex member 10 (MCM10) reported as a cause of NK-cell deficiency in a child with fatal susceptibility to CMV.
Sources: Literature