abnormal long bone epiphysis morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the rounded end of a long bone (Mammalian Phenotype Ontology, MP_0000131)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000131
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25 gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACP5 acid phosphatase 5, tartrate resistant
BGN biglycan
CAV1 caveolin 1, caveolae protein, 22kDa
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
COL2A1 collagen, type II, alpha 1
CST5 cystatin D
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
FGF23 fibroblast growth factor 23
FOS FBJ murine osteosarcoma viral oncogene homolog
FOSL2 FOS-like antigen 2
GDF5 growth differentiation factor 5
HAPLN1 hyaluronan and proteoglycan link protein 1
HELLS helicase, lymphoid-specific
HSPG2 heparan sulfate proteoglycan 2
KL klotho
NCDN neurochondrin
NLRP3 NLR family, pyrin domain containing 3
RUNX2 runt-related transcription factor 2
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLC30A5 solute carrier family 30 (zinc transporter), member 5
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
SLC39A13 solute carrier family 39 (zinc transporter), member 13
SUMF1 sulfatase modifying factor 1
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
TRIP11 thyroid hormone receptor interactor 11