craniosynostosis Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description A synostosis that results_in premature fusion located_in skull. (Human Disease Ontology, DOID_2340)
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Genes

18 genes co-occuring with the biological term craniosynostosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ADAMTSL4 ADAMTS-like 4
ALX4 ALX homeobox 4
BBS9 Bardet-Biedl syndrome 9
BMP2 bone morphogenetic protein 2
CYP26B1 cytochrome P450, family 26, subfamily B, polypeptide 1
FGF1 fibroblast growth factor 1 (acidic)
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
IGF1R insulin-like growth factor 1 receptor
IRS1 insulin receptor substrate 1
MSX2 msh homeobox 2
NELL1 NEL-like 1 (chicken)
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
POR P450 (cytochrome) oxidoreductase
TGFB1 transforming growth factor, beta 1
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
TWIST1 twist family bHLH transcription factor 1