abnormal hyaline cartilage morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the bluish-white, glassy, translucent nonvascular, resilient, flexible connective tissue; found primarily in articular cartilage, costal cartilages, the nasal septum, the larynx, and the trachea (Mammalian Phenotype Ontology, MP_0006429)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006429
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Genes

17 gene mutations causing the abnormal hyaline cartilage morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARSB arylsulfatase B
CAV1 caveolin 1, caveolae protein, 22kDa
COL11A1 collagen, type XI, alpha 1
COL11A2 collagen, type XI, alpha 2
COL2A1 collagen, type II, alpha 1
COL9A1 collagen, type IX, alpha 1
FGFR3 fibroblast growth factor receptor 3
FLNB filamin B, beta
FMOD fibromodulin
GDF5 growth differentiation factor 5
GDF6 growth differentiation factor 6
GUSB glucuronidase, beta
HOXC10 homeobox C10
MMP2 matrix metallopeptidase 2
PRG4 proteoglycan 4
PTH1R parathyroid hormone 1 receptor
SMAD3 SMAD family member 3