abnormal coronal suture morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the dense, fibrous connective tissue joint between the parietal bones and the frontal bone (Mammalian Phenotype Ontology, MP_0003840)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003840
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11 gene mutations causing the abnormal coronal suture morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGF9 fibroblast growth factor 9
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GDF6 growth differentiation factor 6
IFT88 intraflagellar transport 88
ITGB1BP1 integrin beta 1 binding protein 1
KAT6B K(lysine) acetyltransferase 6B
LMNA lamin A/C
LMNB1 lamin B1
MMP2 matrix metallopeptidase 2
VEGFA vascular endothelial growth factor A