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| Retinitis pigmentosa v0.223 | ACTG1 | Zornitza Stark Marked gene: ACTG1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Retinitis pigmentosa v0.223 | ACTG1 | Zornitza Stark Gene: actg1 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Retinitis pigmentosa v0.203 | Bryony Thompson Copied gene ACTG1 from panel Retinitis pigmentosa_Autosomal Dominant | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Retinitis pigmentosa v0.203 | ACTG1 |
Bryony Thompson gene: ACTG1 was added gene: ACTG1 was added to Retinitis pigmentosa_Autosomal Recessive/X-linked. Sources: Expert Review Amber,Literature Mode of inheritance for gene: ACTG1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: ACTG1 were set to PMID: 28000701, PMID 34448047, PMID 39734360 Phenotypes for gene: ACTG1 were set to Retinitis pigmentosa MONDO:0019200, ACTG1-related Mode of pathogenicity for gene: ACTG1 was set to Other |
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