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Possible mitochondrial disorder, nuclear genes v3.113 OXCT1 Achchuthan Shanmugasundram Tag Q3_23_promote_green was removed from gene: OXCT1.
Possible mitochondrial disorder, nuclear genes v3.113 OXCT1 Achchuthan Shanmugasundram commented on gene: OXCT1: The rating of this gene has been updated to green following NHS Genomic Medicine Service approval.
Possible mitochondrial disorder, nuclear genes v3.112 OXCT1 Achchuthan Shanmugasundram Source Expert Review Green was added to OXCT1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Possible mitochondrial disorder, nuclear genes v3.44 OXCT1 Achchuthan Shanmugasundram Classified gene: OXCT1 as Amber List (moderate evidence)
Possible mitochondrial disorder, nuclear genes v3.44 OXCT1 Achchuthan Shanmugasundram Added comment: Comment on list classification: As there is sufficient evidence available, this gene can be promoted to green rating in this panel in the next major update.
Possible mitochondrial disorder, nuclear genes v3.44 OXCT1 Achchuthan Shanmugasundram Gene: oxct1 has been classified as Amber List (Moderate Evidence).
Possible mitochondrial disorder, nuclear genes v3.43 OXCT1 Achchuthan Shanmugasundram Publications for gene: OXCT1 were set to
Possible mitochondrial disorder, nuclear genes v3.42 OXCT1 Achchuthan Shanmugasundram Tag Q3_23_promote_green tag was added to gene: OXCT1.
Possible mitochondrial disorder, nuclear genes v3.42 OXCT1 Achchuthan Shanmugasundram reviewed gene: OXCT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 8751852, 10964512, 11757586, 23420214, 25778941; Phenotypes: Succinyl CoA:3-oxoacid CoA transferase deficiency, OMIM:24505; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v0.5 OXCT1 Ivone Leong reviewed gene: OXCT1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Succinyl CoA:3-oxoacid CoA transferase deficiency, 245050; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Possible mitochondrial disorder, nuclear genes v0.4 OXCT1 Ivone Leong gene: OXCT1 was added
gene: OXCT1 was added to Possible mitochondrial disorder - nuclear genes. Sources: Expert Review Red,NHS GMS
Mode of inheritance for gene: OXCT1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: OXCT1 were set to Succinyl CoA:3-oxoacid CoA transferase deficiency, 245050