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Possible mitochondrial disorder, nuclear genes v3.113 MSTO1 Achchuthan Shanmugasundram Tag Q1_24_MOI was removed from gene: MSTO1.
Possible mitochondrial disorder, nuclear genes v3.113 MSTO1 Achchuthan Shanmugasundram reviewed gene: MSTO1: Rating: ; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v3.112 MSTO1 Achchuthan Shanmugasundram Mode of inheritance for gene MSTO1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v3.89 MSTO1 Sarah Leigh Added comment: Comment on mode of inheritance: The mode of inheritance should be changed to BIALLELIC, autosomal or pseudoautosomal.
Possible mitochondrial disorder, nuclear genes v3.89 MSTO1 Sarah Leigh Mode of inheritance for gene: MSTO1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v3.88 MSTO1 Sarah Leigh Tag Q1_24_MOI tag was added to gene: MSTO1.
Possible mitochondrial disorder, nuclear genes v3.88 MSTO1 Sarah Leigh Publications for gene: MSTO1 were set to 28554942; 28544275; 29339779
Possible mitochondrial disorder, nuclear genes v3.87 MSTO1 Sarah Leigh reviewed gene: MSTO1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v1.40 MSTO1 Sarah Leigh Phenotypes for gene: MSTO1 were changed from Myopathy, mitochondrial, and ataxia, 617675 to Myopathy, mitochondrial, and ataxia OMIM:617675; mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome MONDO:0044714
Possible mitochondrial disorder, nuclear genes v0.155 MSTO1 Ellen McDonagh Marked gene: MSTO1 as ready
Possible mitochondrial disorder, nuclear genes v0.155 MSTO1 Ellen McDonagh Gene: msto1 has been classified as Green List (High Evidence).
Possible mitochondrial disorder, nuclear genes v0.155 MSTO1 Ellen McDonagh Classified gene: MSTO1 as Green List (high evidence)
Possible mitochondrial disorder, nuclear genes v0.155 MSTO1 Ellen McDonagh Added comment: Comment on list classification: This gene was promoted from Amber to Green due to the overall review and evidence assessment from the GMS mitochondrial specialist test group, submitted by Carl Fratter.
Possible mitochondrial disorder, nuclear genes v0.155 MSTO1 Ellen McDonagh Gene: msto1 has been classified as Green List (High Evidence).
Possible mitochondrial disorder, nuclear genes v0.154 MSTO1 Ellen McDonagh Publications for gene: MSTO1 were set to
Possible mitochondrial disorder, nuclear genes v0.134 MSTO1 Carl Fratter reviewed gene: MSTO1: Rating: GREEN; Mode of pathogenicity: ; Publications: 28554942, 28544275, 29339779; Phenotypes: Myopathy, mitochondrial, and ataxia, 617675; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v0.115 MSTO1 Ellen McDonagh Classified gene: MSTO1 as Amber List (moderate evidence)
Possible mitochondrial disorder, nuclear genes v0.115 MSTO1 Ellen McDonagh Added comment: Comment on list classification: This gene has been demoted to Amber until further evidence is provided. This gene is not currently on the Mitochondrial disorders panel (code 112, Version 1.151) - further evidence needs to be submitted to support promoting this gene family member to Green.
Possible mitochondrial disorder, nuclear genes v0.115 MSTO1 Ellen McDonagh Gene: msto1 has been classified as Amber List (Moderate Evidence).
Possible mitochondrial disorder, nuclear genes v0.5 MSTO1 Ivone Leong reviewed gene: MSTO1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Myopathy, mitochondrial, and ataxia, 617675; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v0.2 MSTO1 Ivone Leong gene: MSTO1 was added
gene: MSTO1 was added to Possible mitochondrial disorder - nuclear genes. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: MSTO1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes for gene: MSTO1 were set to Myopathy, mitochondrial, and ataxia, 617675