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Motor Neurone Disease v0.193 DAO Bryony Thompson Marked gene: DAO as ready
Motor Neurone Disease v0.193 DAO Bryony Thompson Gene: dao has been classified as Red List (Low Evidence).
Motor Neurone Disease v0.176 DAO Bryony Thompson Deleted their comment
Motor Neurone Disease v0.176 DAO Bryony Thompson Classified gene: DAO as Red List (low evidence)
Motor Neurone Disease v0.176 DAO Bryony Thompson Added comment: Comment on list classification: Refuted gene-disease validity assessment by ClinGen ALS spectrum disorders GCEP - 21/04/2022
Motor Neurone Disease v0.176 DAO Bryony Thompson Gene: dao has been classified as Red List (Low Evidence).
Motor Neurone Disease v0.176 DAO Bryony Thompson Classified gene: DAO as Red List (low evidence)
Motor Neurone Disease v0.176 DAO Bryony Thompson Added comment: Comment on list classification: Refuted gene-disease vailidity assessment by ClinGen ALS spectrum disorders GCEP - 21/04/2022
Motor Neurone Disease v0.176 DAO Bryony Thompson Gene: dao has been classified as Red List (Low Evidence).
Motor Neurone Disease v0.21 DAO Bryony Thompson gene: DAO was added
gene: DAO was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: DAO was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: DAO were set to 29274788; 29895397; 20368421; 29194436
Phenotypes for gene: DAO were set to Amyotrophic Lateral Sclerosis
Review for gene: DAO was set to RED
Added comment: Many mouse models, but reported variant in a case is R199W, which has gnomAD AF higher than expected for a dominant ALS gene. No compelling evidence in human cases.
Sources: Expert list