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Genetic Epilepsy v2.0 SPOUT1 Gene migrated from ENSG00000198917 to ENSG00000198917 (gene set migration)
Genetic Epilepsy v1.126 SPOUT1 Zornitza Stark Phenotypes for gene: SPOUT1 were changed from complex neurodevelopmental disorder MONDO:0100038, SPOUT1-related to Neurodevelopmental disorder with poor growth, seizures, and brain abnormalities, MIM# 621154
Genetic Epilepsy v1.125 SPOUT1 Zornitza Stark reviewed gene: SPOUT1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder with poor growth, seizures, and brain abnormalities, MIM# 621154; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genetic Epilepsy v1.116 SPOUT1 Bryony Thompson Marked gene: SPOUT1 as ready
Genetic Epilepsy v1.116 SPOUT1 Bryony Thompson Gene: spout1 has been classified as Green List (High Evidence).
Genetic Epilepsy v1.116 SPOUT1 Bryony Thompson Classified gene: SPOUT1 as Green List (high evidence)
Genetic Epilepsy v1.116 SPOUT1 Bryony Thompson Gene: spout1 has been classified as Green List (High Evidence).
Genetic Epilepsy v1.115 SPOUT1 Bryony Thompson Classified gene: SPOUT1 as Green List (high evidence)
Genetic Epilepsy v1.115 SPOUT1 Bryony Thompson Gene: spout1 has been classified as Green List (High Evidence).
Genetic Epilepsy v1.115 SPOUT1 Bryony Thompson Classified gene: SPOUT1 as Green List (high evidence)
Genetic Epilepsy v1.115 SPOUT1 Bryony Thompson Gene: spout1 has been classified as Green List (High Evidence).
Genetic Epilepsy v1.114 SPOUT1 Bryony Thompson gene: SPOUT1 was added
gene: SPOUT1 was added to Genetic Epilepsy. Sources: Literature
Mode of inheritance for gene: SPOUT1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SPOUT1 were set to 39962046
Phenotypes for gene: SPOUT1 were set to complex neurodevelopmental disorder MONDO:0100038, SPOUT1-related
Review for gene: SPOUT1 was set to GREEN
Added comment: Biallelic SPOUT1 variants were identified in 28 individuals with a complex neurodevelopmental disorder from 21 unrelated families. Common phenotypes include microcephaly (18/21), seizures (20/28), intellectual disability (14/14), and varying degrees of developmental delays (28/28). Also, supporting zebrafish model. The suggested name of the disorder is SpADMiSS (SPOUT1 Associated Development delay Microcephaly Seizures Short stature).
Sources: Literature