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Mendeliome v2.620 KIRREL3 Zornitza Stark Phenotypes for gene: KIRREL3 were changed from Intellectual disability MONDO:0001071, KIRREL3-related to complex neurodevelopmental disorder, MONDO:0100038, KIRREL3-related
Mendeliome v2.619 KIRREL3 Zornitza Stark Publications for gene: KIRREL3 were set to 19012874
Mendeliome v2.546 KIRREL3 Sarah Milton reviewed gene: KIRREL3: Rating: RED; Mode of pathogenicity: None; Publications: 42590949; Phenotypes: complex neurodevelopmental disorder, MONDO:0100038, KIRREL3-related; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v2.0 KIRREL3 Gene migrated from ENSG00000149571 to ENSG00000149571 (gene set migration)
Mendeliome v1.4007 KIRREL3 Lucy Spencer Phenotypes for gene: KIRREL3 were changed from Intellectual disability to Intellectual disability MONDO:0001071, KIRREL3-related
Mendeliome v1.3669 KIRREL3 chirag patel reviewed gene: KIRREL3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Mendeliome v1.3669 KIRREL3 chirag patel Tag refuted was removed from gene: KIRREL3.
Tag disputed tag was added to gene: KIRREL3.
Mendeliome v0.4886 KIRREL3 Zornitza Stark Marked gene: KIRREL3 as ready
Mendeliome v0.4886 KIRREL3 Zornitza Stark Gene: kirrel3 has been classified as Red List (Low Evidence).
Mendeliome v0.4886 KIRREL3 Zornitza Stark gene: KIRREL3 was added
gene: KIRREL3 was added to Mendeliome. Sources: Expert list
refuted tags were added to gene: KIRREL3.
Mode of inheritance for gene: KIRREL3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: KIRREL3 were set to 19012874
Phenotypes for gene: KIRREL3 were set to Intellectual disability
Review for gene: KIRREL3 was set to RED
Added comment: Variants associated with ID have now been re-classified based on population frequency.
Sources: Expert list