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| Ataxia - adult onset v0.103 | LMNB1 |
Bryony Thompson changed review comment from: Four unrelated families reported with adult onset cerebellar ataxia as a feature of the condition. Sources: Expert list; to: Four unrelated families reported with adult onset cerebellar ataxia as a feature of the condition. CNV is the only reported cause of the condition. Sources: Expert list |
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| Ataxia - adult onset v0.103 | LMNB1 | Bryony Thompson Tag SV/CNV tag was added to gene: LMNB1. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - adult onset v0.56 | LMNB1 |
Bryony Thompson changed review comment from: Four unrelated families reported with cerebellar ataxia as a feature of the condition. Sources: Expert list; to: Four unrelated families reported with adult onset cerebellar ataxia as a feature of the condition. Sources: Expert list |
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| Ataxia - adult onset v0.56 | LMNB1 | Bryony Thompson Marked gene: LMNB1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - adult onset v0.56 | LMNB1 | Bryony Thompson Gene: lmnb1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - adult onset v0.56 | LMNB1 | Bryony Thompson Classified gene: LMNB1 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - adult onset v0.56 | LMNB1 | Bryony Thompson Gene: lmnb1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - adult onset v0.55 | LMNB1 |
Bryony Thompson gene: LMNB1 was added gene: LMNB1 was added to Ataxia - adult onset. Sources: Expert list Mode of inheritance for gene: LMNB1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: LMNB1 were set to 31695592 Phenotypes for gene: LMNB1 were set to Leukodystrophy, adult-onset, autosomal dominant MIM#169500 Review for gene: LMNB1 was set to GREEN Added comment: Four unrelated families reported with cerebellar ataxia as a feature of the condition. Sources: Expert list |
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