Amyotrophic Lateral Sclerosis 10 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of ALS caused_by mutation located_in TARDBP gene located_in chromosome 1. (Human Disease Ontology, DOID_0060201)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C567429
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Genes

1 genes/proteins associated with the disease Amyotrophic Lateral Sclerosis 10 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
TARDBP TAR DNA binding protein 2.88009