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Mitochondrial disease v0.23 MRPS16 Zornitza Stark Marked gene: MRPS16 as ready
Mitochondrial disease v0.23 MRPS16 Zornitza Stark Gene: mrps16 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.23 MRPS16 Zornitza Stark Classified gene: MRPS16 as Amber List (moderate evidence)
Mitochondrial disease v0.23 MRPS16 Zornitza Stark Added comment: Comment on list classification: Amber for mitochondrial.
Mitochondrial disease v0.23 MRPS16 Zornitza Stark Gene: mrps16 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.23 MRPS16 Zornitza Stark Phenotypes for gene: MRPS16 were changed from to Combined oxidative phosphorylation deficiency 2; OMIM #610498
Mitochondrial disease v0.22 MRPS16 Zornitza Stark Publications for gene: MRPS16 were set to
Mitochondrial disease v0.22 MRPS16 Zornitza Stark Mode of inheritance for gene: MRPS16 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.22 MRPS16 Zornitza Stark Classified gene: MRPS16 as Amber List (moderate evidence)
Mitochondrial disease v0.22 MRPS16 Zornitza Stark Added comment: Comment on list classification: Amber for mitochondrial.
Mitochondrial disease v0.22 MRPS16 Zornitza Stark Gene: mrps16 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.0 MRPS16 Zornitza Stark gene: MRPS16 was added
gene: MRPS16 was added to Mitochondrial_AGHA_VCGS. Sources: Expert Review Green,Australian Genomics Health Alliance Mitochondrial Flagship,Victorian Clinical Genetics Services
Mode of inheritance for gene: MRPS16 was set to Unknown