| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Cerebral Palsy v1.232 | TBR1 | Zornitza Stark Marked gene: TBR1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cerebral Palsy v1.232 | TBR1 | Zornitza Stark Gene: tbr1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cerebral Palsy v1.232 | TBR1 | Zornitza Stark Classified gene: TBR1 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cerebral Palsy v1.232 | TBR1 | Zornitza Stark Gene: tbr1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cerebral Palsy v1.194 | TBR1 |
Clare van Eyk gene: TBR1 was added gene: TBR1 was added to Cerebral Palsy. Sources: Literature Mode of inheritance for gene: TBR1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: TBR1 were set to PMID: 38693247 Phenotypes for gene: TBR1 were set to Intellectual developmental disorder with autism and speech delay, MIM#606053 Review for gene: TBR1 was set to RED Added comment: 1 individual with mono-allelic LOF (frameshift deletion) reported in large-scale exome sequencing study (PMID: 38693247). No additional clinical information provided. Sources: Literature |
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