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Mitochondrial disorder with complex III deficiency v1.4 UQCR11 Arina Puzriakova Classified gene: UQCR11 as Red List (low evidence)
Mitochondrial disorder with complex III deficiency v1.4 UQCR11 Arina Puzriakova Added comment: Comment on list classification: Demoting to Red as there is no evidence for Mendelian gene-disease association at this time
Mitochondrial disorder with complex III deficiency v1.4 UQCR11 Arina Puzriakova Gene: uqcr11 has been classified as Red List (Low Evidence).
Mitochondrial disorder with complex III deficiency v0.19 UQCR11 Ellen McDonagh Marked gene: UQCR11 as ready
Mitochondrial disorder with complex III deficiency v0.19 UQCR11 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 III deficiency v0.19 UQCR11 Ellen McDonagh Gene: uqcr11 has been classified as Amber List (Moderate Evidence).
Mitochondrial disorder with complex III deficiency v0.16 UQCR11 Carl Fratter reviewed gene: UQCR11: Rating: AMBER; Mode of pathogenicity: ; Publications: none found; Phenotypes: No OMIM phenotype; Mode of inheritance: Unknown
Mitochondrial disorder with complex III deficiency v0.13 UQCR11 Anna de Burca Classified gene: UQCR11 as Amber List (moderate evidence)
Mitochondrial disorder with complex III deficiency v0.13 UQCR11 Anna de Burca Gene: uqcr11 has been classified as Amber List (Moderate Evidence).
Mitochondrial disorder with complex III deficiency v0.3 UQCR11 Ivone Leong reviewed gene: UQCR11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: No OMIM phenotype; Mode of inheritance: Unknown
Mitochondrial disorder with complex III deficiency v0.2 UQCR11 Ivone Leong gene: UQCR11 was added
gene: UQCR11 was added to Mitochondrial disorder with complex III deficiency. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: UQCR11 was set to Unknown
Phenotypes for gene: UQCR11 were set to No OMIM phenotype