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Skeletal dysplasia v1.0 GPX4 Gene migrated from ENSG00000167468 to ENSG00000167468 (gene set migration)
Skeletal dysplasia v0.150 GPX4 Ain Roesley changed review comment from: PMID: 24706940
2x families.
The first, maternally inherited splice and a de novo splice
The second is a consaguineous family was a hom nonsense but DNA from deceased infant and parents were sequenced

PMID: 32827718
1x consaguineous family with 2x infants who died within first week of life. Hom for a fs variant; to: PMID: 24706940
2x families.
The first, maternally inherited splice and a de novo splice
The second is a consaguineous family was a hom nonsense but DNA from deceased infant was unavailable and parents were sequenced

PMID: 32827718
1x consaguineous family with 2x infants who died within first week of life. Hom for a fs variant
Skeletal dysplasia v0.150 GPX4 Zornitza Stark Marked gene: GPX4 as ready
Skeletal dysplasia v0.150 GPX4 Zornitza Stark Gene: gpx4 has been classified as Green List (High Evidence).
Skeletal dysplasia v0.150 GPX4 Zornitza Stark Phenotypes for gene: GPX4 were changed from Spondylometaphyseal dysplasia, Sedaghatian type 250220 to Spondylometaphyseal dysplasia, Sedaghatian type MIM#250220
Skeletal dysplasia v0.149 GPX4 Zornitza Stark Publications for gene: GPX4 were set to 24706940
Skeletal dysplasia v0.148 GPX4 Zornitza Stark Classified gene: GPX4 as Green List (high evidence)
Skeletal dysplasia v0.148 GPX4 Zornitza Stark Gene: gpx4 has been classified as Green List (High Evidence).
Skeletal dysplasia v0.147 GPX4 Ain Roesley reviewed gene: GPX4: Rating: GREEN; Mode of pathogenicity: None; Publications: 24706940, 32827718; Phenotypes: Spondylometaphyseal dysplasia, Sedaghatian type MIM#250220; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Skeletal dysplasia v0.0 GPX4 Zornitza Stark gene: GPX4 was added
gene: GPX4 was added to Skeletal dysplasia. Sources: NHS GMS,Expert Review Amber,Expert list,Radboud University Medical Center, Nijmegen
Mode of inheritance for gene: GPX4 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GPX4 were set to 24706940
Phenotypes for gene: GPX4 were set to Spondylometaphyseal dysplasia, Sedaghatian type 250220