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Mendeliome v1.1900 ABCA1 Katrina Bell Deleted their comment
Mendeliome v1.1900 ABCA1 Katrina Bell Added comment: Comment on phenotypes: asdasfcd
Mendeliome v1.1900 ABCA1 Katrina Bell Phenotypes for gene: ABCA1 were changed from Tangier disease, MIM# 205400; HDL deficiency, familial, 1, MIM# 604091 to Tangier disease, MIM# 205400; HDL deficiency, familial, 1, MIM# 604091
Mendeliome v1.1899 ABCA1 Katrina Bell Classified gene: ABCA1 as Green List (high evidence)
Mendeliome v1.1899 ABCA1 Katrina Bell Added comment: Comment on list classification: fsfdeswfd
Mendeliome v1.1899 ABCA1 Katrina Bell Classified gene: ABCA1 as Green List (high evidence)
Mendeliome v1.1899 ABCA1 Katrina Bell Added comment: Comment on list classification: fsfdeswfd
Mendeliome v1.1899 ABCA1 Katrina Bell Gene: abca1 has been classified as Green List (High Evidence).
Mendeliome v1.1899 ABCA1 Katrina Bell Gene: abca1 has been classified as Green List (High Evidence).
Mendeliome v1.1898 ABCA1 Katrina Bell Classified gene: ABCA1 as Green List (high evidence)
Mendeliome v1.1898 ABCA1 Katrina Bell Added comment: Comment on list classification: fsfdeswfd
Mendeliome v1.1898 ABCA1 Katrina Bell Gene: abca1 has been classified as Green List (High Evidence).
Mendeliome v1.1897 ABCA1 Katrina Bell Deleted their comment
Mendeliome v1.1897 ABCA1 Katrina Bell Deleted their comment
Mendeliome v1.1897 ABCA1 Katrina Bell Deleted their comment
Mendeliome v1.1897 ABCA1 Katrina Bell Classified gene: ABCA1 as Amber List (moderate evidence)
Mendeliome v1.1897 ABCA1 Katrina Bell Added comment: Comment on list classification: bdsbbdb db sdfb
Mendeliome v1.1897 ABCA1 Katrina Bell Gene: abca1 has been classified as Amber List (Moderate Evidence).
Mendeliome v1.1896 ABCA1 Katrina Bell Added comment: Comment on publications: x x vxc v x
Mendeliome v1.1896 ABCA1 Katrina Bell Publications for gene: ABCA1 were set to 10431237; 10431236
Mendeliome v1.1896 ABCA1 Katrina Bell Added comment: Comment on publications: x x vxc v x
Mendeliome v1.1896 ABCA1 Katrina Bell Publications for gene: ABCA1 were set to 10431237; 10431236
Mendeliome v1.1895 ABCA1 Katrina Bell Classified gene: ABCA1 as Amber List (moderate evidence)
Mendeliome v1.1895 ABCA1 Katrina Bell Added comment: Comment on list classification: bdsbbdb db sdfb
Mendeliome v1.1895 ABCA1 Katrina Bell Gene: abca1 has been classified as Amber List (Moderate Evidence).
Mendeliome v1.1895 ABCA1 Katrina Bell Added comment: Comment on publications: x x vxc v x
Mendeliome v1.1895 ABCA1 Katrina Bell Publications for gene: ABCA1 were set to 10431237; 10431236
Mendeliome v1.1894 ABCA1 Katrina Bell Classified gene: ABCA1 as Amber List (moderate evidence)
Mendeliome v1.1894 ABCA1 Katrina Bell Added comment: Comment on list classification: bdsbbdb db sdfb
Mendeliome v1.1894 ABCA1 Katrina Bell Gene: abca1 has been classified as Amber List (Moderate Evidence).
Mendeliome v1.1894 ABCA1 Katrina Bell Classified gene: ABCA1 as Amber List (moderate evidence)
Mendeliome v1.1894 ABCA1 Katrina Bell Added comment: Comment on list classification: bdsbbdb db sdfb
Mendeliome v1.1894 ABCA1 Katrina Bell Gene: abca1 has been classified as Amber List (Moderate Evidence).
Mendeliome v1.1894 ABCA1 Katrina Bell Mode of inheritance for gene: ABCA1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Mendeliome v1.1893 ABCA1 Katrina Bell Added comment: Comment on mode of pathogenicity: cznjc n jzklcv jlcxzjcv lbzjxkc lbzjcl bjkz
Mendeliome v1.1893 ABCA1 Katrina Bell Mode of pathogenicity for gene: ABCA1 was changed from Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Mendeliome v1.1893 ABCA1 Katrina Bell Added comment: Comment on mode of pathogenicity: cznjc n jzklcv jlcxzjcv lbzjxkc lbzjcl bjkz
Mendeliome v1.1893 ABCA1 Katrina Bell Mode of pathogenicity for gene: ABCA1 was changed from Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Mendeliome v1.1892 ABCA1 Katrina Bell Added comment: Comment on mode of pathogenicity: cznjc n jzklcv jlcxzjcv lbzjxkc lbzjcl bjkz
Mendeliome v1.1892 ABCA1 Katrina Bell Mode of pathogenicity for gene: ABCA1 was changed from to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Mendeliome v1.1891 ABCA1 Katrina Bell commented on gene: ABCA1
Mendeliome v0.7340 ABCA1 Zornitza Stark Marked gene: ABCA1 as ready
Mendeliome v0.7340 ABCA1 Zornitza Stark Gene: abca1 has been classified as Green List (High Evidence).
Mendeliome v0.4012 ABCA12 Zornitza Stark Marked gene: ABCA12 as ready
Mendeliome v0.4012 ABCA12 Zornitza Stark Gene: abca12 has been classified as Green List (High Evidence).
Mendeliome v0.4012 ABCA12 Zornitza Stark Phenotypes for gene: ABCA12 were changed from to Ichthyosis, congenital, autosomal recessive 4A (MIM#601277); Ichthyosis, congenital, autosomal recessive 4B (harlequin) (MIM#242500)
Mendeliome v0.4011 ABCA12 Zornitza Stark Publications for gene: ABCA12 were set to
Mendeliome v0.4010 ABCA12 Zornitza Stark Mode of inheritance for gene: ABCA12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.4009 ABCA12 Zornitza Stark reviewed gene: ABCA12: Rating: GREEN; Mode of pathogenicity: None; Publications: 31168818, 19664001, 31489029; Phenotypes: Ichthyosis, congenital, autosomal recessive 4A (MIM#601277), Ichthyosis, congenital, autosomal recessive 4B (harlequin) (MIM#242500); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.4009 ABCA1 Zornitza Stark Phenotypes for gene: ABCA1 were changed from to Tangier disease, MIM# 205400; HDL deficiency, familial, 1, MIM# 604091
Mendeliome v0.4008 ABCA1 Zornitza Stark Publications for gene: ABCA1 were set to
Mendeliome v0.4007 ABCA1 Zornitza Stark Mode of inheritance for gene: ABCA1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendeliome v0.4006 ABCA1 Zornitza Stark reviewed gene: ABCA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10431237, 10431236; Phenotypes: Tangier disease, MIM# 205400, HDL deficiency, familial, 1, MIM# 604091; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendeliome v0.0 ABCA12 Zornitza Stark gene: ABCA12 was added
gene: ABCA12 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ABCA12 was set to Unknown
Mendeliome v0.0 ABCA1 Zornitza Stark gene: ABCA1 was added
gene: ABCA1 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ABCA1 was set to Unknown