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Confirmed Fanconi anaemia or Bloom syndrome v0.20 SLX4 Louise Daugherty commented on gene: SLX4: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SLX4; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Fanconi Anemia;Fanconi anemia, complementation group P, 613951; PMID(s): none submitted
Confirmed Fanconi anaemia or Bloom syndrome v0.19 SLX4 Steve Keeney reviewed gene: SLX4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Fanconi Anemia, Fanconi anemia, complementation group P, 613951; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Confirmed Fanconi anaemia or Bloom syndrome v0.18 SLX4 Louise Daugherty Added phenotypes Fanconi Anemia; Fanconi anemia, complementation group P, 613951 for gene: SLX4
Confirmed Fanconi anaemia or Bloom syndrome v0.16 SLX4 Louise Daugherty Source North West GLH was added to SLX4.
Confirmed Fanconi anaemia or Bloom syndrome v0.11 SLX4 Louise Daugherty commented on gene: SLX4: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SLX4; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 613951 Fanconi Anemia Fanconi anemia, complementation group P; PMID(s): none submitted
Confirmed Fanconi anaemia or Bloom syndrome v0.10 SLX4 Mandy nesbitt reviewed gene: SLX4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 613951 Fanconi Anemia Fanconi anemia, complementation group P; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Confirmed Fanconi anaemia or Bloom syndrome v0.9 SLX4 Louise Daugherty Added phenotypes 613951 Fanconi Anemia Fanconi anemia, complementation group P for gene: SLX4
Confirmed Fanconi anaemia or Bloom syndrome v0.7 SLX4 Louise Daugherty Source Yorkshire and North East GLH was added to SLX4.
Confirmed Fanconi anaemia or Bloom syndrome v0.6 SLX4 Louise Daugherty reviewed gene: SLX4: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Confirmed Fanconi anaemia or Bloom syndrome v0.5 SLX4 Carl Fratter reviewed gene: SLX4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Confirmed Fanconi anaemia or Bloom syndrome v0.4 SLX4 Louise Daugherty Source NHS GMS was added to SLX4.
Confirmed Fanconi anaemia or Bloom syndrome v0.3 SLX4 Louise Daugherty Source Expert Review Green was added to SLX4.
Mode of inheritance for gene SLX4 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Fanconi Anemia; Fanconi anemia, complementation group P, 613951 for gene: SLX4
Publications for gene SLX4 were changed from to 21240275; 21240277
Rating Changed from Red List (low evidence) to Green List (high evidence)
Confirmed Fanconi anaemia or Bloom syndrome v0.2 SLX4 Louise Daugherty gene: SLX4 was added
gene: SLX4 was added to Confirmed Fanconi anaemia or Bloom syndrome. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: SLX4 was set to