| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Genetic Epilepsy v0.2201 | TMEM5 | Elena Savva Marked gene: TMEM5 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2201 | TMEM5 | Elena Savva Gene: tmem5 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2201 | TMEM5 |
Elena Savva gene: TMEM5 was added gene: TMEM5 was added to Genetic Epilepsy. Sources: Literature Mode of inheritance for gene: TMEM5 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: TMEM5 were set to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10 MIM#615041 Review for gene: TMEM5 was set to RED Added comment: Alt, gene name RXYLT1 No literature showing SNVs in this gene and epilepsy/seizures. Gene was listed in the Oliver review Sources: Literature |
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