disorganized long bone epiphyseal plate Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a lack of the regular arrangement of the cells or zones of the epiphyseal plate (Mammalian Phenotype Ontology, MP_0006397)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006397
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21 gene mutations causing the disorganized long bone epiphyseal plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACP5 acid phosphatase 5, tartrate resistant
ARSB arylsulfatase B
ATF2 activating transcription factor 2
COL11A2 collagen, type XI, alpha 2
COL2A1 collagen, type II, alpha 1
CRTAP cartilage associated protein
CSGALNACT1 chondroitin sulfate N-acetylgalactosaminyltransferase 1
CTGF connective tissue growth factor
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
DYM dymeclin
FGFR3 fibroblast growth factor receptor 3
FOS FBJ murine osteosarcoma viral oncogene homolog
HSPG2 heparan sulfate proteoglycan 2
IFT80 intraflagellar transport 80
IMPAD1 inositol monophosphatase domain containing 1
KIF3A kinesin family member 3A
NLRP3 NLR family, pyrin domain containing 3
NPPC natriuretic peptide C
NPR2 natriuretic peptide receptor 2
PHEX phosphate regulating endopeptidase homolog, X-linked
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor