| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Cone-rod Dystrophy v0.11 | OPN1SW | Zornitza Stark Marked gene: OPN1SW as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cone-rod Dystrophy v0.11 | OPN1SW | Zornitza Stark Gene: opn1sw has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cone-rod Dystrophy v0.3 | OPN1SW | Bryony Thompson Classified gene: OPN1SW as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cone-rod Dystrophy v0.3 | OPN1SW | Bryony Thompson Gene: opn1sw has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cone-rod Dystrophy v0.2 | OPN1SW |
Bryony Thompson gene: OPN1SW was added gene: OPN1SW was added to Cone-rod Dystrophy. Sources: Expert list Mode of inheritance for gene: OPN1SW was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: OPN1SW were set to 22065927; 1531728 Phenotypes for gene: OPN1SW were set to Colorblindness, tritan MIM#190900 Review for gene: OPN1SW was set to GREEN Added comment: Has been included on this panel, so that it is with the other cone-specific colour blindness genes. At least 6 missense variants associated with tritanopia. Sources: Expert list |
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