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Dystonia, chorea or related movement disorder, childhood onset v3.51 FOXG1 Arina Puzriakova Publications for gene: FOXG1 were set to 21441262; 19564653; 19578037; 27029630
Dystonia, chorea or related movement disorder, childhood onset v1.217 FOXG1 Sarah Leigh commented on gene: FOXG1: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Dystonia, chorea or related movement disorder, childhood onset v1.212 FOXG1 Sarah Leigh Tag Q2_21_rating was removed from gene: FOXG1.
Dystonia, chorea or related movement disorder, childhood onset v1.212 FOXG1 Sarah Leigh commented on gene: FOXG1: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Dystonia, chorea or related movement disorder, childhood onset v1.211 FOXG1 Sarah Leigh Source Expert Review Green was added to FOXG1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Dystonia, chorea or related movement disorder, childhood onset v1.122 FOXG1 Sarah Leigh Tag Q2_21_rating tag was added to gene: FOXG1.
Dystonia, chorea or related movement disorder, childhood onset v1.122 FOXG1 Sarah Leigh edited their review of gene: FOXG1: Added comment: Associated with relevant phenotype in OMIM and as confirmed Gen2Phen gene. All of the patients with FOXG1 variants reported in PMID 27029630 abnormal involuntary movements, including chorea/athetosis in 22/25 (88%) cases.; Changed rating: GREEN
Dystonia, chorea or related movement disorder, childhood onset v1.122 FOXG1 Sarah Leigh Publications for gene: FOXG1 were set to 27029630
Dystonia, chorea or related movement disorder, childhood onset v1.121 FOXG1 Sarah Leigh Classified gene: FOXG1 as Amber List (moderate evidence)
Dystonia, chorea or related movement disorder, childhood onset v1.121 FOXG1 Sarah Leigh Added comment: Comment on list classification: There is enough evidence for this gene to be rated GREEN at the next major review.
Dystonia, chorea or related movement disorder, childhood onset v1.121 FOXG1 Sarah Leigh Gene: foxg1 has been classified as Amber List (Moderate Evidence).
Dystonia, chorea or related movement disorder, childhood onset v1.120 FOXG1 Sarah Leigh Phenotypes for gene: FOXG1 were changed from Rett Syndrome, congenital variant, 613454 to Rett Syndrome, congenital variant OMIM:613454; Rett syndrome, congenital variant MONDO:0013270
Dystonia, chorea or related movement disorder, childhood onset v1.119 FOXG1 Sarah Leigh Publications for gene: FOXG1 were set to
Dystonia, chorea or related movement disorder, childhood onset v1.49 FOXG1 Zornitza Stark reviewed gene: FOXG1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27029630; Phenotypes: Rett syndrome, congenital variant, MIM# 613454; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Dystonia, chorea or related movement disorder, childhood onset v0.12 FOXG1 Ellen McDonagh Classified gene: FOXG1 as Amber List (moderate evidence)
Dystonia, chorea or related movement disorder, childhood onset v0.12 FOXG1 Ellen McDonagh Added comment: Comment on list classification: Promoted from Red to Amber due to review from North Bristol NHS Trust.
Dystonia, chorea or related movement disorder, childhood onset v0.12 FOXG1 Ellen McDonagh Gene: foxg1 has been classified as Amber List (Moderate Evidence).
Dystonia, chorea or related movement disorder, childhood onset v0.1 FOXG1 Ellen McDonagh gene: FOXG1 was added
gene: FOXG1 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: South West GLH
Mode of inheritance for gene: FOXG1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: FOXG1 were set to Rett Syndrome, congenital variant, 613454