Gene: HSPG2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3339
Gene Symbol: HSPG2
HSPG2 		0.010 GeneticVariation disease BEFREE We propose that the decreased binding affinity of NOG with the p.R136C mutation to HSPG leads to an excess of BMP signaling and underlies the SYM1 and conductive hearing loss phenotype of carriers. 24735539 2014