Coffin-Lowry Syndrome Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_3783)
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Genes

3 genes associated with the Coffin-Lowry Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
COL2A1 collagen, type II, alpha 1
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
WRN Werner syndrome, RecQ helicase-like