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Hereditary Spastic Paraplegia v2.5 GSN chirag patel Marked gene: GSN as ready
Hereditary Spastic Paraplegia v2.5 GSN chirag patel Gene: gsn has been classified as Red List (Low Evidence).
Hereditary Spastic Paraplegia v2.5 GSN chirag patel Publications for gene: GSN were set to 2176164; 28139293
Hereditary Spastic Paraplegia v2.4 GSN chirag patel Phenotypes for gene: GSN were changed from Spastic ataxia, MONDO:0017845, GSN-related to Spastic ataxia, MONDO:0017845, GSN-related
Hereditary Spastic Paraplegia v2.4 GSN chirag patel Mode of inheritance for gene: GSN was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary Spastic Paraplegia v2.4 GSN chirag patel Mode of inheritance for gene: GSN was changed from BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary Spastic Paraplegia v2.3 GSN chirag patel Phenotypes for gene: GSN were changed from Amyloidosis, Finnish type, MIM# 105120; Spastic ataxia, MONDO:0017845, GSN-related to Spastic ataxia, MONDO:0017845, GSN-related
Hereditary Spastic Paraplegia v2.3 GSN chirag patel Classified gene: GSN as Red List (low evidence)
Hereditary Spastic Paraplegia v2.3 GSN chirag patel Gene: gsn has been classified as Red List (Low Evidence).
Hereditary Spastic Paraplegia v2.2 chirag patel Copied gene GSN from panel Mendeliome
Hereditary Spastic Paraplegia v2.2 GSN chirag patel gene: GSN was added
gene: GSN was added to Hereditary Spastic Paraplegia. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: GSN was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Publications for gene: GSN were set to 2176164; 28139293
Phenotypes for gene: GSN were set to Amyloidosis, Finnish type, MIM# 105120; Spastic ataxia, MONDO:0017845, GSN-related