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Mendeliome v0.5112 COX14 Zornitza Stark Phenotypes for gene: COX14 were changed from Mitochondrial complex IV deficiency, MIM#220110 to Mitochondrial complex IV deficiency, nuclear type 10, MIM#619053
Mendeliome v0.5111 COX14 Zornitza Stark edited their review of gene: COX14: Changed phenotypes: Mitochondrial complex IV deficiency, nuclear type 10, MIM#619053
Mendeliome v0.109 COX14 Zornitza Stark Marked gene: COX14 as ready
Mendeliome v0.109 COX14 Zornitza Stark Gene: cox14 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.109 COX14 Zornitza Stark Phenotypes for gene: COX14 were changed from to Mitochondrial complex IV deficiency, MIM#220110
Mendeliome v0.108 COX14 Zornitza Stark Publications for gene: COX14 were set to
Mendeliome v0.107 COX14 Zornitza Stark Mode of inheritance for gene: COX14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.106 COX14 Zornitza Stark Classified gene: COX14 as Amber List (moderate evidence)
Mendeliome v0.106 COX14 Zornitza Stark Gene: cox14 has been classified as Amber List (Moderate Evidence).
Mendeliome v0.0 COX14 Zornitza Stark gene: COX14 was added
gene: COX14 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: COX14 was set to Unknown