| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Congenital Heart Defect v0.499 | PROX1 | Chirag Patel Marked gene: PROX1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v0.499 | PROX1 | Chirag Patel Gene: prox1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v0.499 | PROX1 |
Chirag Patel gene: PROX1 was added gene: PROX1 was added to Congenital Heart Defect. Sources: ClinGen disputed tags were added to gene: PROX1. Mode of inheritance for gene: PROX1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: PROX1 were set to Congenital heart disease, MONDO:0005453 Review for gene: PROX1 was set to RED Added comment: ClinGen DISPUTED - Aug 2024 Sources: ClinGen |
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