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Ataxia and cerebellar anomalies - narrow panel v4.38 INTS11 Arina Puzriakova Phenotypes for gene: INTS11 were changed from Complex neurodevelopmental disorder, MONDO:0100038 to Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities, OMIM:620428
Ataxia and cerebellar anomalies - narrow panel v4.37 INTS11 Achchuthan Shanmugasundram Tag Q2_23_promote_green was removed from gene: INTS11.
Ataxia and cerebellar anomalies - narrow panel v4.37 INTS11 Eleanor Williams reviewed gene: INTS11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ataxia and cerebellar anomalies - narrow panel v4.35 INTS11 Achchuthan Shanmugasundram Source Expert Review Green was added to INTS11.
Source NHS GMS was added to INTS11.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Ataxia and cerebellar anomalies - narrow panel v4.11 INTS11 Arina Puzriakova Entity copied from Intellectual disability - microarray and sequencing v5.151
Ataxia and cerebellar anomalies - narrow panel v4.11 INTS11 Arina Puzriakova gene: INTS11 was added
gene: INTS11 was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Amber,Literature
Q2_23_promote_green tags were added to gene: INTS11.
Mode of inheritance for gene: INTS11 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: INTS11 were set to 37054711
Phenotypes for gene: INTS11 were set to Complex neurodevelopmental disorder, MONDO:0100038