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Combined Immunodeficiency v2.0 LCK Gene migrated from ENSG00000182866 to ENSG00000182866 (gene set migration)
Combined Immunodeficiency v1.56 LCK Zornitza Stark Publications for gene: LCK were set to 22985903; 1579166; 11021796
Combined Immunodeficiency v1.55 LCK Zornitza Stark Classified gene: LCK as Green List (high evidence)
Combined Immunodeficiency v1.55 LCK Zornitza Stark Gene: lck has been classified as Green List (High Evidence).
Combined Immunodeficiency v1.54 LCK Peter McNaughton reviewed gene: LCK: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 38100037, PMID: 27087313; Phenotypes: Combined Immune deficiency; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Combined Immunodeficiency v0.245 LCK Zornitza Stark Marked gene: LCK as ready
Combined Immunodeficiency v0.245 LCK Zornitza Stark Gene: lck has been classified as Amber List (Moderate Evidence).
Combined Immunodeficiency v0.245 LCK Zornitza Stark Phenotypes for gene: LCK were changed from to Immunodeficiency 22 MIM# 615758; Recurrent infections; Immune dysregulation; autoimmunity; Low CD4+; low CD8+; restricted T cell repertoire; poor TCR signaling; Normal IgG/IgA; high IgM; failure to thrive; diarrhoea; lymphopenia; hypogammaglobulinemia; anaemia; thrombocytopaenia; CD4+ T-cell lymphopenia
Combined Immunodeficiency v0.244 LCK Zornitza Stark Publications for gene: LCK were set to
Combined Immunodeficiency v0.243 LCK Zornitza Stark Mode of inheritance for gene: LCK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Combined Immunodeficiency v0.242 LCK Zornitza Stark Classified gene: LCK as Amber List (moderate evidence)
Combined Immunodeficiency v0.242 LCK Zornitza Stark Gene: lck has been classified as Amber List (Moderate Evidence).
Combined Immunodeficiency v0.232 LCK Danielle Ariti reviewed gene: LCK: Rating: AMBER; Mode of pathogenicity: None; Publications: 22985903, 1579166, 11021796; Phenotypes: Immunodeficiency 22 MIM# 615758, Recurrent infections, Immune dysregulation, autoimmunity, Low CD4+, low CD8+, restricted T cell repertoire, poor TCR signaling, Normal IgG/IgA, high IgM, failure to thrive, diarrhoea, lymphopenia, hypogammaglobulinemia, anaemia, thrombocytopaenia, CD4+ T-cell lymphopenia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Combined Immunodeficiency v0.0 LCK Zornitza Stark gene: LCK was added
gene: LCK was added to Combined immunodeficiency_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship
Mode of inheritance for gene: LCK was set to Unknown