| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Auditory Neuropathy v0.13 | MPZ | Bryony Thompson Marked gene: MPZ as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Auditory Neuropathy v0.13 | MPZ | Bryony Thompson Gene: mpz has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Auditory Neuropathy v0.13 | MPZ | Bryony Thompson Publications for gene: MPZ were set to 21176974 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Auditory Neuropathy v0.12 | MPZ | Bryony Thompson reviewed gene: MPZ: Rating: RED; Mode of pathogenicity: None; Publications: 12845552, 12805115; Phenotypes: Syndromic auditory neuropathy spectrum disorder; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Auditory Neuropathy v0.0 | MPZ |
Bryony Thompson gene: MPZ was added gene: MPZ was added to Auditory Neuropathy. Sources: Literature Mode of inheritance for gene: MPZ was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: MPZ were set to 21176974 Phenotypes for gene: MPZ were set to Syndromic auditory neuropathy spectrum disorder |
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