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| Hereditary Spastic Paraplegia - adult onset v0.120 | ATP2B4 | Zornitza Stark Marked gene: ATP2B4 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia - adult onset v0.120 | ATP2B4 | Zornitza Stark Gene: atp2b4 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia - adult onset v0.120 | ATP2B4 | Zornitza Stark Mode of inheritance for gene: ATP2B4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia - adult onset v0.6 | ATP2B4 | Bryony Thompson reviewed gene: ATP2B4: Rating: AMBER; Mode of pathogenicity: None; Publications: 25119969, 25798335, 29691679; Phenotypes: Hereditary spastic paraplegia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia - adult onset v0.0 | ATP2B4 |
Bryony Thompson gene: ATP2B4 was added gene: ATP2B4 was added to Hereditary Spastic Paraplegia - adult onset_RMH. Sources: Expert Review Amber,Royal Melbourne Hospital Mode of inheritance for gene: ATP2B4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: ATP2B4 were set to 29691679; 25798335; 25119969 Phenotypes for gene: ATP2B4 were set to Pure and complicated hereditary spastic paraplegia |
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