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| Ataxia - adult onset v0.146 | RNF170 | Zornitza Stark Marked gene: RNF170 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - adult onset v0.146 | RNF170 | Zornitza Stark Gene: rnf170 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - adult onset v0.146 | RNF170 | Zornitza Stark Phenotypes for gene: RNF170 were changed from Ataxia, sensory, 1, autosomal dominant; Autosomal dominant sensory ataxia 1, 608984 to Ataxia, sensory, 1, autosomal dominant, MIM# 608984 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - adult onset v0.145 | RNF170 | Zornitza Stark Publications for gene: RNF170 were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - adult onset v0.144 | RNF170 | Zornitza Stark Mode of inheritance for gene: RNF170 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - adult onset v0.143 | RNF170 | Zornitza Stark reviewed gene: RNF170: Rating: GREEN; Mode of pathogenicity: None; Publications: 32943585, 21115467; Phenotypes: Ataxia, sensory, 1, autosomal dominant, MIM# 608984; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia - adult onset v0.0 | RNF170 |
Bryony Thompson gene: RNF170 was added gene: RNF170 was added to Ataxia - adult onset_RMH. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: RNF170 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: RNF170 were set to Ataxia, sensory, 1, autosomal dominant; Autosomal dominant sensory ataxia 1, 608984 |
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