Amyotrophic Lateral Sclerosis 8 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of ALS caused_by mutation located_in VAPB gene located_in chromosome 20. (Human Disease Ontology, DOID_0050752)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C563895
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Genes

1 genes/proteins associated with the disease Amyotrophic Lateral Sclerosis 8 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
VAPB VAMP (vesicle-associated membrane protein)-associated protein B and C 2.88009