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| Retinitis pigmentosa v1.0 | FSCN2 | Gene migrated from ENSG00000186765 to ENSG00000186765 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Retinitis pigmentosa v0.208 | Bryony Thompson Copied gene FSCN2 from panel Retinitis pigmentosa_Autosomal Dominant | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Retinitis pigmentosa v0.208 | FSCN2 |
Bryony Thompson gene: FSCN2 was added gene: FSCN2 was added to Retinitis pigmentosa_Autosomal Recessive/X-linked. Sources: Expert Review Red,Royal Melbourne Hospital,Royal Melbourne Hospital Mode of inheritance for gene: FSCN2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: FSCN2 were set to 16043865; 18450588 Phenotypes for gene: FSCN2 were set to Retinitis pigmentosa 30 MIM#607921; Macular degeneration |
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