generalized joint laxity Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Joint hypermobility (ability of a joint to move beyond its normal range of motion) affecting many or all joints of the body. (Human Phenotype Ontology, HP_0002761)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0002761
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Genes

5 genes associated with the generalized joint laxity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
CHST14	carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
COMP	cartilage oligomeric matrix protein
FGFR3	fibroblast growth factor receptor 3
KDM6A	lysine (K)-specific demethylase 6A
SERPINH1	serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)