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Possible mitochondrial disorder, nuclear genes v3.113 COX11 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: COX11.
Tag Q4_23_NHS_review was removed from gene: COX11.
Possible mitochondrial disorder, nuclear genes v3.113 COX11 Achchuthan Shanmugasundram reviewed gene: COX11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v3.112 COX11 Achchuthan Shanmugasundram Source Expert Review Green was added to COX11.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Possible mitochondrial disorder, nuclear genes v3.81 COX11 Sarah Leigh Classified gene: COX11 as Amber List (moderate evidence)
Possible mitochondrial disorder, nuclear genes v3.81 COX11 Sarah Leigh Added comment: Comment on list classification: There is enough evidence for this gene to be rated GREEN at the next major review.
Possible mitochondrial disorder, nuclear genes v3.81 COX11 Sarah Leigh Gene: cox11 has been classified as Amber List (Moderate Evidence).
Possible mitochondrial disorder, nuclear genes v3.80 COX11 Sarah Leigh Tag Q4_23_promote_green tag was added to gene: COX11.
Tag Q4_23_NHS_review tag was added to gene: COX11.
Possible mitochondrial disorder, nuclear genes v3.80 COX11 Sarah Leigh reviewed gene: COX11: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Possible mitochondrial disorder, nuclear genes v3.80 COX11 Sarah Leigh Mode of inheritance for gene: COX11 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v3.79 COX11 Sarah Leigh Phenotypes for gene: COX11 were changed from Mitochondrial complex IV deficiency, nuclear type 23, OMIM:620275; Mitochondrial complex IV deficiency, nuclear type 23, MONDO:0859520 to Mitochondrial complex IV deficiency, nuclear type 23, OMIM:620275; Mitochondrial complex IV deficiency, nuclear type 23, MONDO:0859520
Possible mitochondrial disorder, nuclear genes v3.78 COX11 Sarah Leigh Publications for gene: COX11 were set to 36030551; 38068960
Possible mitochondrial disorder, nuclear genes v3.77 COX11 Sarah Leigh Publications for gene: COX11 were set to 36030551
Possible mitochondrial disorder, nuclear genes v3.76 COX11 Sarah Leigh Publications for gene: COX11 were set to
Possible mitochondrial disorder, nuclear genes v3.75 COX11 Sarah Leigh Mode of inheritance for gene: COX11 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v3.74 COX11 Sarah Leigh Phenotypes for gene: COX11 were changed from No OMIM phenotype to Mitochondrial complex IV deficiency, nuclear type 23, OMIM:620275; Mitochondrial complex IV deficiency, nuclear type 23, MONDO:0859520
Possible mitochondrial disorder, nuclear genes v3.48 COX11 Hannah Knight reviewed gene: COX11: Rating: AMBER; Mode of pathogenicity: None; Publications: 36030551; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 23; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v0.148 COX11 Ellen McDonagh Marked gene: COX11 as ready
Possible mitochondrial disorder, nuclear genes v0.148 COX11 Ellen McDonagh Added comment: Comment when marking as ready: This gene should remain Amber due to the overall review and evidence assessment from the GMS mitochondrial specialist test group, submitted by Carl Fratter.
Possible mitochondrial disorder, nuclear genes v0.148 COX11 Ellen McDonagh Gene: cox11 has been classified as Amber List (Moderate Evidence).
Possible mitochondrial disorder, nuclear genes v0.134 COX11 Carl Fratter reviewed gene: COX11: Rating: AMBER; Mode of pathogenicity: ; Publications: no mito reports found; Phenotypes: No OMIM phenotype; Mode of inheritance: Unknown
Possible mitochondrial disorder, nuclear genes v0.89 COX11 Ellen McDonagh Classified gene: COX11 as Amber List (moderate evidence)
Possible mitochondrial disorder, nuclear genes v0.89 COX11 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 v0.89 COX11 Ellen McDonagh Gene: cox11 has been classified as Amber List (Moderate Evidence).
Possible mitochondrial disorder, nuclear genes v0.5 COX11 Ivone Leong reviewed gene: COX11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: No OMIM phenotype; Mode of inheritance: Unknown
Possible mitochondrial disorder, nuclear genes v0.2 COX11 Ivone Leong gene: COX11 was added
gene: COX11 was added to Possible mitochondrial disorder - nuclear genes. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: COX11 was set to Unknown
Phenotypes for gene: COX11 were set to No OMIM phenotype