Activity

Filter

Cancel
Date Panel Item Activity
13 actions
Early onset or syndromic epilepsy v8.166 MARK2 Ida Ertmanska Added comment: Comment on phenotypes: Phenotype updated 20 Mar 2026.
Early onset or syndromic epilepsy v8.166 MARK2 Ida Ertmanska Phenotypes for gene: MARK2 were changed from neurodevelopmental disorder, MONDO:0700092; intellectual disability, MONDO:0001071 to Intellectual developmental disorder, autosomal dominant 76, OMIM:621285; intellectual developmental disorder, autosomal dominant 76, MONDO:0979575
Early onset or syndromic epilepsy v8.165 MARK2 Ida Ertmanska Tag gene-checked was removed from gene: MARK2.
Early onset or syndromic epilepsy v8.139 MARK2 Arina Puzriakova Tag Q1_25_ promote_green was removed from gene: MARK2.
Early onset or syndromic epilepsy v8.134 MARK2 Achchuthan Shanmugasundram commented on gene: MARK2: The rating of this gene has been updated to green following NHS Genomic Medicine Service approval.
Early onset or syndromic epilepsy v8.134 MARK2 Arina Puzriakova Source Expert Review Green was added to MARK2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Early onset or syndromic epilepsy v7.54 MARK2 Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: MARK2.
Early onset or syndromic epilepsy v7.51 MARK2 Arina Puzriakova Classified gene: MARK2 as Amber List (moderate evidence)
Early onset or syndromic epilepsy v7.51 MARK2 Arina Puzriakova Gene: mark2 has been classified as Amber List (Moderate Evidence).
Early onset or syndromic epilepsy v7.50 MARK2 Sarah Leigh Deleted their comment
Early onset or syndromic epilepsy v7.50 MARK2 Arina Puzriakova Tag Q1_25_ promote_green tag was added to gene: MARK2.
Early onset or syndromic epilepsy v7.50 MARK2 Arina Puzriakova Entity copied from Intellectual disability v8.126
Early onset or syndromic epilepsy v7.50 MARK2 Arina Puzriakova gene: MARK2 was added
gene: MARK2 was added to Early onset or syndromic epilepsy. Sources: Expert Review Green,NHS GMS,Literature
Mode of inheritance for gene: MARK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MARK2 were set to 39419027; 39436150
Phenotypes for gene: MARK2 were set to neurodevelopmental disorder, MONDO:0700092; intellectual disability, MONDO:0001071