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Radial Ray Abnormalities v0.78 ESCO2 Zornitza Stark Phenotypes for gene: ESCO2 were changed from Roberts syndrome 268300; SC phocomelia syndrome 269000 to Roberts syndrome 268300; SC phocomelia syndrome 269000; Juberg-Hayward syndrome, MIM# 216100
Radial Ray Abnormalities v0.77 ESCO2 Zornitza Stark Publications for gene: ESCO2 were set to 19574259; 16380922
Radial Ray Abnormalities v0.76 ESCO2 Zornitza Stark reviewed gene: ESCO2: Rating: GREEN; Mode of pathogenicity: None; Publications: 32977150; Phenotypes: Juberg-Hayward syndrome, MIM# 216100, Roberts-SC phocomelia syndrome, MIM#268300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Radial Ray Abnormalities v0.13 ESCO2 Seb Lunke Marked gene: ESCO2 as ready
Radial Ray Abnormalities v0.13 ESCO2 Seb Lunke Gene: esco2 has been classified as Green List (High Evidence).
Radial Ray Abnormalities v0.13 ESCO2 Seb Lunke Publications for gene: ESCO2 were set to PMID: 19574259; 16380922
Radial Ray Abnormalities v0.12 ESCO2 Seb Lunke Classified gene: ESCO2 as Green List (high evidence)
Radial Ray Abnormalities v0.12 ESCO2 Seb Lunke Gene: esco2 has been classified as Green List (High Evidence).
Radial Ray Abnormalities v0.11 ESCO2 Natalie Tan changed review comment from: Sources: NHS GMS; to: Sources: NHS GMS

Multiple unrelated individuals with biallelic variants in association with Roberts syndrome/SC phocomelia spectrum.
Radial Ray Abnormalities v0.11 ESCO2 Natalie Tan gene: ESCO2 was added
gene: ESCO2 was added to Radial Ray Abnormalities. Sources: NHS GMS
Mode of inheritance for gene: ESCO2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ESCO2 were set to PMID: 19574259; 16380922
Phenotypes for gene: ESCO2 were set to Roberts syndrome 268300; SC phocomelia syndrome 269000
Review for gene: ESCO2 was set to GREEN
Added comment: Sources: NHS GMS