| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Syndromic Retinopathy v0.60 | SCLT1 | Bryony Thompson Marked gene: SCLT1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Syndromic Retinopathy v0.60 | SCLT1 | Bryony Thompson Gene: sclt1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Syndromic Retinopathy v0.60 | SCLT1 | Bryony Thompson Classified gene: SCLT1 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Syndromic Retinopathy v0.60 | SCLT1 | Bryony Thompson Gene: sclt1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Syndromic Retinopathy v0.59 | SCLT1 |
Bryony Thompson gene: SCLT1 was added gene: SCLT1 was added to Syndromic Retinopathy. Sources: Expert list Mode of inheritance for gene: SCLT1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SCLT1 were set to 32253632; 30425282 Phenotypes for gene: SCLT1 were set to Bardet Biedl syndrome; Senior-Loken syndrome Review for gene: SCLT1 was set to GREEN Added comment: Three unrelated cases reported with retinal dystrophy as a feature of the condition (2 with BBS and 1 with SLS). Sources: Expert list |
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