Activity

Filter

Cancel
Date Panel Item Activity
8 actions
Microcephaly v1.125 SLC38A3 Zornitza Stark Phenotypes for gene: SLC38A3 were changed from Developmental epileptic encephalopathy MONDO:0100062, SLC38A3-related to Developmental and epileptic encephalopathy 102, MIM# 619881
Microcephaly v1.124 SLC38A3 Zornitza Stark reviewed gene: SLC38A3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Developmental and epileptic encephalopathy 102, MIM# 619881; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Microcephaly v1.100 SLC38A3 Zornitza Stark Marked gene: SLC38A3 as ready
Microcephaly v1.100 SLC38A3 Zornitza Stark Gene: slc38a3 has been classified as Green List (High Evidence).
Microcephaly v1.100 SLC38A3 Zornitza Stark Phenotypes for gene: SLC38A3 were changed from developmental epileptic encephalopathy, SLC38A3-related MONDO:0100062 to Developmental epileptic encephalopathy MONDO:0100062, SLC38A3-related
Microcephaly v1.99 SLC38A3 Zornitza Stark Classified gene: SLC38A3 as Green List (high evidence)
Microcephaly v1.99 SLC38A3 Zornitza Stark Gene: slc38a3 has been classified as Green List (High Evidence).
Microcephaly v1.98 SLC38A3 Ain Roesley gene: SLC38A3 was added
gene: SLC38A3 was added to Microcephaly. Sources: Literature
Mode of inheritance for gene: SLC38A3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC38A3 were set to 34605855
Phenotypes for gene: SLC38A3 were set to developmental epileptic encephalopathy, SLC38A3-related MONDO:0100062
Penetrance for gene: SLC38A3 were set to Complete
Review for gene: SLC38A3 was set to GREEN
gene: SLC38A3 was marked as current diagnostic
Added comment: 7 families 6 of whom are consanguineous but unique variants in all of them

Acquired microcephaly noted (8/10 with >-2 SD, 5/10 >-3 SD)
Sources: Literature