Gene: RPS6KA3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6197
Gene Symbol: RPS6KA3
RPS6KA3 		0.020 Biomarker disease BEFREE In the near vicinity to the associated region, RPS6KA3 was identified as a candidate gene causing facial dysmorphia in humans and mice known as Coffin-Lowry syndrome. 31691328 2020
Entrez Id: 6197
Gene Symbol: RPS6KA3
RPS6KA3 		0.020 GeneticVariation disease BEFREE Coffin-Lowry syndrome is an X-linked mental retardation disorder with dysmorphism caused by mutation of the ribosomal S6 kinase (RSK2) gene. 15668050 2005