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| Mendeliome v1.3081 | KCNA4 | Zornitza Stark Marked gene: KCNA4 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v1.3081 | KCNA4 | Zornitza Stark Gene: kcna4 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v1.3081 | KCNA4 |
Zornitza Stark gene: KCNA4 was added gene: KCNA4 was added to Mendeliome. Sources: Literature Mode of inheritance for gene: KCNA4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: KCNA4 were set to 40472070 Phenotypes for gene: KCNA4 were set to Epilepsy, MONDO:0005027, KCNA4-related Review for gene: KCNA4 was set to RED Added comment: Single individual with de novo missense variant reported. Sources: Literature |
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