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Dystonia - complex v0.232 MAPT Bryony Thompson edited their review of gene: MAPT: Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Dystonia - complex v0.102 MAPT Zornitza Stark Marked gene: MAPT as ready
Dystonia - complex v0.102 MAPT Zornitza Stark Gene: mapt has been classified as Amber List (Moderate Evidence).
Dystonia - complex v0.102 MAPT Zornitza Stark Classified gene: MAPT as Amber List (moderate evidence)
Dystonia - complex v0.102 MAPT Zornitza Stark Gene: mapt has been classified as Amber List (Moderate Evidence).
Dystonia - complex v0.26 MAPT Bryony Thompson gene: MAPT was added
gene: MAPT was added to Dystonia - complex. Sources: Expert list
Mode of inheritance for gene: MAPT was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MAPT were set to 17319286; 15883319
Phenotypes for gene: MAPT were set to Dementia, frontotemporal, with or without parkinsonism MIM#600274
Review for gene: MAPT was set to AMBER
Added comment: Dystonia has been reported in two cases. Cannot find evidence that dystonia is a prominent feature associated with MAPT variants.
Sources: Expert list