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Genetic Epilepsy v2.0 ADGRL1 Gene migrated from ENSG00000072071 to ENSG00000072071 (gene set migration)
Genetic Epilepsy v0.1695 ADGRL1 Zornitza Stark Phenotypes for gene: ADGRL1 were changed from Neurodevelopmental disorder, ADGRL1-related (MONDO#0700092) to Developmental delay, behavioral abnormalities, and neuropsychiatric disorders, MIM# 620065
Genetic Epilepsy v0.1694 ADGRL1 Zornitza Stark reviewed gene: ADGRL1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Developmental delay, behavioral abnormalities, and neuropsychiatric disorders, MIM# 620065; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genetic Epilepsy v0.1638 ADGRL1 Elena Savva Classified gene: ADGRL1 as Amber List (moderate evidence)
Genetic Epilepsy v0.1638 ADGRL1 Elena Savva Gene: adgrl1 has been classified as Amber List (Moderate Evidence).
Genetic Epilepsy v0.1637 ADGRL1 Elena Savva Classified gene: ADGRL1 as Amber List (moderate evidence)
Genetic Epilepsy v0.1637 ADGRL1 Elena Savva Gene: adgrl1 has been classified as Amber List (Moderate Evidence).
Genetic Epilepsy v0.1637 ADGRL1 Elena Savva Classified gene: ADGRL1 as Amber List (moderate evidence)
Genetic Epilepsy v0.1637 ADGRL1 Elena Savva Gene: adgrl1 has been classified as Amber List (Moderate Evidence).
Genetic Epilepsy v0.1636 ADGRL1 Elena Savva Marked gene: ADGRL1 as ready
Genetic Epilepsy v0.1636 ADGRL1 Elena Savva Gene: adgrl1 has been classified as Red List (Low Evidence).
Genetic Epilepsy v0.1636 ADGRL1 Elena Savva gene: ADGRL1 was added
gene: ADGRL1 was added to Genetic Epilepsy. Sources: Literature
Mode of inheritance for gene: ADGRL1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: ADGRL1 were set to PMID: 35907405
Phenotypes for gene: ADGRL1 were set to Neurodevelopmental disorder, ADGRL1-related (MONDO#0700092)
Review for gene: ADGRL1 was set to AMBER
Added comment: PMID: 35907405 - 9 patients, only had epilepsy (2/9).

Het null mouse model shows neurological and developmental abnormalities, with hom null mice non-viable.
Sources: Literature