abnormal head fold morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the crescent-shaped, ventrally located fold of the embryonic disc at the future cephalic end of the developing embryo; it constitutes the first body fold, and initiates brain, foregut and heart development (Mammalian Phenotype Ontology, MP_0011257)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011257
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8 gene mutations causing the abnormal head fold morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CRB2 crumbs family member 2
CTDNEP1 CTD nuclear envelope phosphatase 1
FGFR1 fibroblast growth factor receptor 1
LEFTY2 left-right determination factor 2
NODAL nodal growth differentiation factor
PRKCI protein kinase C, iota
PTK2 protein tyrosine kinase 2
SMAD2 SMAD family member 2