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Prepair 500+ v1.1015 SCO2 Zornitza Stark Marked gene: SCO2 as ready
Prepair 500+ v1.1015 SCO2 Zornitza Stark Gene: sco2 has been classified as Green List (High Evidence).
Prepair 500+ v1.1015 SCO2 Zornitza Stark Phenotypes for gene: SCO2 were changed from Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1, 604377 (3) to Mitochondrial complex IV deficiency, nuclear type 2 MIM#604377
Prepair 500+ v1.1014 SCO2 Zornitza Stark Publications for gene: SCO2 were set to
Prepair 500+ v1.352 ESCO2 Zornitza Stark Marked gene: ESCO2 as ready
Prepair 500+ v1.352 ESCO2 Zornitza Stark Gene: esco2 has been classified as Green List (High Evidence).
Prepair 500+ v1.352 ESCO2 Zornitza Stark Phenotypes for gene: ESCO2 were changed from SC phocomelia syndrome, 269000 (3) to Roberts-SC phocomelia syndrome (MIM#268300)
Prepair 500+ v1.351 ESCO2 Zornitza Stark Publications for gene: ESCO2 were set to
Prepair 500+ v0.0 SCO2 Seb Lunke gene: SCO2 was added
gene: SCO2 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green
Mode of inheritance for gene: SCO2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: SCO2 were set to Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1, 604377 (3)
Prepair 500+ v0.0 ESCO2 Seb Lunke gene: ESCO2 was added
gene: ESCO2 was added to Prepair 500+. Sources: Mackenzie's Mission,Expert Review Green
Mode of inheritance for gene: ESCO2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ESCO2 were set to SC phocomelia syndrome, 269000 (3)