short fibula Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the fibula. (Human Phenotype Ontology, HP_0003038)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002765
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Genes

17 gene mutations causing the short fibula phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGF9 fibroblast growth factor 9
GDF5 growth differentiation factor 5
GLI2 GLI family zinc finger 2
GLI3 GLI family zinc finger 3
IFT172 intraflagellar transport 172
IHH indian hedgehog
KIAA1715 KIAA1715
NPPC natriuretic peptide C
PHEX phosphate regulating endopeptidase homolog, X-linked
PRRX1 paired related homeobox 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
RSPO2 R-spondin 2
RYK receptor-like tyrosine kinase
SHH sonic hedgehog
SMOC1 SPARC related modular calcium binding 1
VKORC1 vitamin K epoxide reductase complex, subunit 1
WNT7A wingless-type MMTV integration site family, member 7A