premature bone ossification Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description early onset of the formation of bone (Mammalian Phenotype Ontology, MP_0003416)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003416
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Genes

21 gene mutations causing the premature bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AXIN2 axin 2
CAV1 caveolin 1, caveolae protein, 22kDa
CNN1 calponin 1, basic, smooth muscle
DUSP6 dual specificity phosphatase 6
ERF Ets2 repressor factor
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FREM1 FRAS1 related extracellular matrix 1
GLI3 GLI family zinc finger 3
HDAC4 histone deacetylase 4
IGF2R insulin-like growth factor 2 receptor
LTBP3 latent transforming growth factor beta binding protein 3
NSDHL NAD(P) dependent steroid dehydrogenase-like
PRDM16 PR domain containing 16
PTHLH parathyroid hormone-like hormone
TGFBR1 transforming growth factor, beta receptor 1
THBS3 thrombospondin 3
THRB thyroid hormone receptor, beta
TWIST1 twist family bHLH transcription factor 1
XYLT1 xylosyltransferase I
Funding