decreased width of hypertrophic chondrocyte zone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decreased width of cartilage cell matrix layer (Mammalian Phenotype Ontology, MP_0003409)
External Link
Similar Terms
Downloads & Tools


33 gene mutations causing the decreased width of hypertrophic chondrocyte zone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
COL2A1 collagen, type II, alpha 1
CREB3L2 cAMP responsive element binding protein 3-like 2
CSGALNACT1 chondroitin sulfate N-acetylgalactosaminyltransferase 1
DYM dymeclin
EGR2 early growth response 2
EVC Ellis van Creveld protein
EVC2 Ellis van Creveld syndrome 2
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FOSL2 FOS-like antigen 2
GHR growth hormone receptor
IFT80 intraflagellar transport 80
IGF1 insulin-like growth factor 1 (somatomedin C)
IHH indian hedgehog
ITGA10 integrin, alpha 10
LGALS3 lectin, galactoside-binding, soluble, 3
MEX3C mex-3 RNA binding family member C
MGP matrix Gla protein
NLRP3 NLR family, pyrin domain containing 3
NPPC natriuretic peptide C
NPR2 natriuretic peptide receptor 2
PAPSS2 3'-phosphoadenosine 5'-phosphosulfate synthase 2
PKD1 polycystic kidney disease 1 (autosomal dominant)
PRKCD protein kinase C, delta
PRRX1 paired related homeobox 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
SIK3 SIK family kinase 3
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
SNAP25 synaptosomal-associated protein, 25kDa
SPRED2 sprouty-related, EVH1 domain containing 2
THRA thyroid hormone receptor, alpha
TWSG1 twisted gastrulation BMP signaling modulator 1
XYLT1 xylosyltransferase I