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| Motor Neurone Disease v0.35 | UBQLN4 | Bryony Thompson Classified gene: UBQLN4 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Motor Neurone Disease v0.35 | UBQLN4 | Bryony Thompson Gene: ubqln4 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Motor Neurone Disease v0.34 | UBQLN4 |
Bryony Thompson gene: UBQLN4 was added gene: UBQLN4 was added to Motor Neuron Disease. Sources: Expert list Mode of inheritance for gene: UBQLN4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: UBQLN4 were set to 28463112; 30804504 Phenotypes for gene: UBQLN4 were set to Amyotrophic lateral sclerosis Review for gene: UBQLN4 was set to AMBER Added comment: A single familial case and supporting functional studies and animal model. Sources: Expert list |
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