| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Genetic Epilepsy v0.2106 | ODC1 | Zornitza Stark Publications for gene: ODC1 were set to PMID:30475435; 30239107 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2105 | ODC1 | Zornitza Stark edited their review of gene: ODC1: Changed rating: RED | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2094 | ODC1 | Lauren Rogers reviewed gene: ODC1: Rating: RED; Mode of pathogenicity: None; Publications: 34477286; Phenotypes: Bachmann-Bupp syndrome MIM#619075; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1347 | ODC1 | Zornitza Stark Marked gene: ODC1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1347 | ODC1 | Zornitza Stark Gene: odc1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1347 | ODC1 | Zornitza Stark Classified gene: ODC1 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1347 | ODC1 | Zornitza Stark Gene: odc1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1340 | ODC1 |
Belinda Chong changed review comment from: Epilepsy appears to be a rare feature of this syndrome. Sources: Literature; to: Epilepsy not reported. Sources: Literature |
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| Genetic Epilepsy v0.1317 | ODC1 |
Belinda Chong gene: ODC1 was added gene: ODC1 was added to Genetic Epilepsy. Sources: Literature Mode of inheritance for gene: ODC1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: ODC1 were set to PMID:30475435; 30239107 Phenotypes for gene: ODC1 were set to Bachmann-Bupp syndrome 619075 Review for gene: ODC1 was set to RED gene: ODC1 was marked as current diagnostic Added comment: Epilepsy appears to be a rare feature of this syndrome. Sources: Literature |
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