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Additional findings_Paediatric v0.95 GRXCR1 Zornitza Stark Marked gene: GRXCR1 as ready
Additional findings_Paediatric v0.95 GRXCR1 Zornitza Stark Gene: grxcr1 has been classified as Green List (High Evidence).
Additional findings_Paediatric v0.95 GRXCR1 Zornitza Stark Phenotypes for gene: GRXCR1 were changed from Deafness, autosomal recessive to Deafness, autosomal recessive 25, MIM# 613285
Additional findings_Paediatric v0.94 GRXCR1 Zornitza Stark Publications for gene: GRXCR1 were set to
Additional findings_Paediatric v0.93 GRXCR1 Zornitza Stark Classified gene: GRXCR1 as Green List (high evidence)
Additional findings_Paediatric v0.93 GRXCR1 Zornitza Stark Gene: grxcr1 has been classified as Green List (High Evidence).
Additional findings_Paediatric v0.92 GRXCR1 Zornitza Stark reviewed gene: GRXCR1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20137778, 25802247, 26226137, 26445815, 26969326, 20137774; Phenotypes: Deafness, autosomal recessive 25, MIM# 613285; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Additional findings_Paediatric v0.2 GRXCR1 Zornitza Stark gene: GRXCR1 was added
gene: GRXCR1 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red
Mode of inheritance for gene: GRXCR1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: GRXCR1 were set to Deafness, autosomal recessive