AMYOTROPHIC LATERAL SCLEROSIS 12 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of ALS caused_by mutation located_in OPTN gene located_in chromosome 10. (Human Disease Ontology, DOID_0060203)
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:613435
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Genes

1 genes/proteins associated with the disease AMYOTROPHIC LATERAL SCLEROSIS 12 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
OPTN optineurin 2.88009