| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Genetic Epilepsy v0.2106 | OGT | Zornitza Stark edited their review of gene: OGT: Changed rating: GREEN | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2106 | OGT | Zornitza Stark edited their review of gene: OGT: Changed rating: RED | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2097 | OGT | Elena Savva Publications for gene: OGT were set to PMID: 28302723; 28584052; 31296563; 31627256; 29769320; 29606577 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2096 | OGT | Lauren Rogers reviewed gene: OGT: Rating: RED; Mode of pathogenicity: None; Publications: 29769320, 37334838; Phenotypes: Intellectual developmental disorder, X-linked 106 MIM#300997; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1343 | OGT | Zornitza Stark Marked gene: OGT as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1343 | OGT | Zornitza Stark Gene: ogt has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1343 | OGT | Zornitza Stark Classified gene: OGT as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1343 | OGT | Zornitza Stark Gene: ogt has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.1337 | OGT |
Belinda Chong changed review comment from: Epilepsy appears to be a rare feature of this disorder. Sources: Literature; to: Epilepsy not reported Sources: Literature |
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| Genetic Epilepsy v0.1336 | OGT |
Belinda Chong changed review comment from: Epilepsy appears to be a rare feature of this syndrome. Sources: Literature; to: Epilepsy appears to be a rare feature of this disorder. Sources: Literature |
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| Genetic Epilepsy v0.1317 | OGT |
Belinda Chong gene: OGT was added gene: OGT was added to Genetic Epilepsy. Sources: Literature Mode of inheritance for gene: OGT was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females Publications for gene: OGT were set to PMID: 28302723; 28584052; 31296563; 31627256; 29769320; 29606577 Phenotypes for gene: OGT were set to Intellectual developmental disorder, X-linked 106 MIM#300997 Review for gene: OGT was set to RED gene: OGT was marked as current diagnostic Added comment: Epilepsy appears to be a rare feature of this syndrome. Sources: Literature |
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