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Radial Ray Abnormalities v2.0 FGFR2 Gene migrated from ENSG00000066468 to ENSG00000066468 (gene set migration)
Radial Ray Abnormalities v0.150 FGFR2 Zornitza Stark Marked gene: FGFR2 as ready
Radial Ray Abnormalities v0.150 FGFR2 Zornitza Stark Gene: fgfr2 has been classified as Green List (High Evidence).
Radial Ray Abnormalities v0.150 FGFR2 Zornitza Stark Classified gene: FGFR2 as Green List (high evidence)
Radial Ray Abnormalities v0.150 FGFR2 Zornitza Stark Gene: fgfr2 has been classified as Green List (High Evidence).
Radial Ray Abnormalities v0.65 FGFR2 Zornitza Stark gene: FGFR2 was added
gene: FGFR2 was added to Radial Ray Abnormalities. Sources: Expert list
Mode of inheritance for gene: FGFR2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: FGFR2 were set to LADD syndrome, MIM#149730
Review for gene: FGFR2 was set to GREEN
Added comment: Well established gene-disease association. Radial ray abnormalities are a feature of LADD syndrome.
Sources: Expert list