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Mitochondrial disorder with complex IV deficiency v0.38 COX7C Ellen McDonagh Marked gene: COX7C as ready
Mitochondrial disorder with complex IV deficiency v0.38 COX7C 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.
Mitochondrial disorder with complex IV deficiency v0.38 COX7C Ellen McDonagh Gene: cox7c has been classified as Amber List (Moderate Evidence).
Mitochondrial disorder with complex IV deficiency v0.38 COX7C Ellen McDonagh Publications for gene: COX7C were set to
Mitochondrial disorder with complex IV deficiency v0.31 COX7C Carl Fratter reviewed gene: COX7C: Rating: AMBER; Mode of pathogenicity: ; Publications: 30634555; Phenotypes: No OMIM phenotype; Mode of inheritance: Unknown
Mitochondrial disorder with complex IV deficiency v0.27 COX7C Ellen McDonagh Classified gene: COX7C as Amber List (moderate evidence)
Mitochondrial disorder with complex IV deficiency v0.27 COX7C Ellen McDonagh Added comment: Comment on list classification: This gene has been demoted to Amber until further evidence is provided. This gene is currently Red on the Mitochondrial disorders panel (code 112, Version 1.132) - further evidence needs to be submitted to support promoting this gene family member to Green.
Mitochondrial disorder with complex IV deficiency v0.27 COX7C Ellen McDonagh Gene: cox7c has been classified as Amber List (Moderate Evidence).
Mitochondrial disorder with complex IV deficiency v0.3 COX7C Ivone Leong reviewed gene: COX7C: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: No OMIM phenotype; Mode of inheritance: Unknown
Mitochondrial disorder with complex IV deficiency v0.2 COX7C Ivone Leong gene: COX7C was added
gene: COX7C was added to Mitochondrial disorder with complex IV deficiency. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: COX7C was set to Unknown
Phenotypes for gene: COX7C were set to No OMIM phenotype