coronal craniosynostosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Premature closure of the coronal suture of skull. (Human Phenotype Ontology, HP_0004440)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004440
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Genes

10 genes associated with the coronal craniosynostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCBE1 collagen and calcium binding EGF domains 1
EFNB1 ephrin-B1
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
IMPAD1 inositol monophosphatase domain containing 1
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
RAB23 RAB23, member RAS oncogene family
RECQL4 RecQ protein-like 4
TWIST1 twist family bHLH transcription factor 1