Activity

Filter

Cancel
Date Panel Item Activity
8 actions
Motor Neurone Disease v0.182 GLT8D1 Bryony Thompson Marked gene: GLT8D1 as ready
Motor Neurone Disease v0.182 GLT8D1 Bryony Thompson Gene: glt8d1 has been classified as Amber List (Moderate Evidence).
Motor Neurone Disease v0.182 GLT8D1 Bryony Thompson Classified gene: GLT8D1 as Amber List (moderate evidence)
Motor Neurone Disease v0.182 GLT8D1 Bryony Thompson Gene: glt8d1 has been classified as Amber List (Moderate Evidence).
Motor Neurone Disease v0.138 GLT8D1 Sarah Leigh reviewed gene: GLT8D1: Rating: AMBER; Mode of pathogenicity: None; Publications: 30811981, 35525134:33581933:31653410:33714647:34746377; Phenotypes: familial amyotrophic lateral sclerosis, MONDO:0005144; Mode of inheritance: None
Motor Neurone Disease v0.23 GLT8D1 Bryony Thompson Classified gene: GLT8D1 as Green List (high evidence)
Motor Neurone Disease v0.23 GLT8D1 Bryony Thompson Gene: glt8d1 has been classified as Green List (High Evidence).
Motor Neurone Disease v0.22 GLT8D1 Bryony Thompson gene: GLT8D1 was added
gene: GLT8D1 was added to Motor Neuron Disease. Sources: Expert list
Mode of inheritance for gene: GLT8D1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: GLT8D1 were set to 30811981
Phenotypes for gene: GLT8D1 were set to Amyotrophic lateral sclerosis
Review for gene: GLT8D1 was set to GREEN
Added comment: 14 ALS cases with heterozygous missense (10 cases with p.R92C), and supporting in vitro functional assays and zebrafish model.
Sources: Expert list