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Genomic newborn screening: BabyScreen+ v0.599 VLDLR Zornitza Stark Marked gene: VLDLR as ready
Genomic newborn screening: BabyScreen+ v0.599 VLDLR Zornitza Stark Gene: vldlr has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.599 VLDLR Zornitza Stark Phenotypes for gene: VLDLR were changed from Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 to Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion MIM#224050
Genomic newborn screening: BabyScreen+ v0.598 VLDLR Zornitza Stark Classified gene: VLDLR as Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.598 VLDLR Zornitza Stark Gene: vldlr has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.588 VLDLR Lilian Downie reviewed gene: VLDLR: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion MIM#224050; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.0 VLDLR Zornitza Stark gene: VLDLR was added
gene: VLDLR was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: VLDLR was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: VLDLR were set to Cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1