| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Retinitis pigmentosa_Autosomal Dominant v0.9 | ARL3 | Bryony Thompson Classified gene: ARL3 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Retinitis pigmentosa_Autosomal Dominant v0.9 | ARL3 | Bryony Thompson Gene: arl3 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Retinitis pigmentosa_Autosomal Dominant v0.8 | ARL3 | Bryony Thompson reviewed gene: ARL3: Rating: AMBER; Mode of pathogenicity: None; Publications: 26964041, 30932721; Phenotypes: Retinitis pigmentosa 83 MIM#618173; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Retinitis pigmentosa_Autosomal Dominant v0.0 | ARL3 |
Bryony Thompson gene: ARL3 was added gene: ARL3 was added to Autosomal Dominant Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green Mode of inheritance for gene: ARL3 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: ARL3 were set to 26936825; 16565502; 26964041; 26814127; 30932721; 30269812 Phenotypes for gene: ARL3 were set to Retinitis pigmentosa 83; Joubert syndrome 35 |
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