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)