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Mitochondrial disorder with complex III deficiency v1.5 UQCC1 Arina Puzriakova Classified gene: UQCC1 as Red List (low evidence)
Mitochondrial disorder with complex III deficiency v1.5 UQCC1 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 v1.5 UQCC1 Arina Puzriakova Gene: uqcc1 has been classified as Red List (Low Evidence).
Mitochondrial disorder with complex III deficiency v0.16 UQCC1 Ellen McDonagh Marked gene: UQCC1 as ready
Mitochondrial disorder with complex III deficiency v0.16 UQCC1 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 v0.16 UQCC1 Ellen McDonagh Gene: uqcc1 has been classified as Amber List (Moderate Evidence).
Mitochondrial disorder with complex III deficiency v0.16 UQCC1 Carl Fratter reviewed gene: UQCC1: Rating: AMBER; Mode of pathogenicity: ; Publications: none found; Phenotypes: No OMIM phenotype; Mode of inheritance: Unknown
Mitochondrial disorder with complex III deficiency v0.15 UQCC1 Anna de Burca Classified gene: UQCC1 as Amber List (moderate evidence)
Mitochondrial disorder with complex III deficiency v0.15 UQCC1 Anna de Burca Gene: uqcc1 has been classified as Amber List (Moderate Evidence).
Mitochondrial disorder with complex III deficiency v0.3 UQCC1 Ivone Leong reviewed gene: UQCC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: No OMIM phenotype; Mode of inheritance: Unknown
Mitochondrial disorder with complex III deficiency v0.2 UQCC1 Ivone Leong gene: UQCC1 was added
gene: UQCC1 was added to Mitochondrial disorder with complex III deficiency. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: UQCC1 was set to Unknown
Phenotypes for gene: UQCC1 were set to No OMIM phenotype