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BabyScreen+ newborn screening v1.114 SIX3 Tommy Li Added phenotypes Holoprosencephaly 2, MIM# 157170 for gene: SIX3
BabyScreen+ newborn screening v0.708 SIX3 Seb Lunke Marked gene: SIX3 as ready
BabyScreen+ newborn screening v0.708 SIX3 Seb Lunke Gene: six3 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.708 SIX3 Seb Lunke Phenotypes for gene: SIX3 were changed from Holoprosencephaly-2 to Holoprosencephaly 2, MIM# 157170
BabyScreen+ newborn screening v0.707 SIX3 Seb Lunke Classified gene: SIX3 as Red List (low evidence)
BabyScreen+ newborn screening v0.707 SIX3 Seb Lunke Gene: six3 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.706 SIX3 Seb Lunke reviewed gene: SIX3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Holoprosencephaly 2, MIM# 157170; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
BabyScreen+ newborn screening v0.0 SIX3 Zornitza Stark gene: SIX3 was added
gene: SIX3 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: SIX3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: SIX3 were set to Holoprosencephaly-2