absent prechordal mesoderm Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of or failure to form the area of axial mesoderm that develops into the prechordal plate (Mammalian Phenotype Ontology, MP_0012276)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012276
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3 gene mutations causing the absent prechordal mesoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXH1 forkhead box H1
LHX1 LIM homeobox 1
OTX2 orthodenticle homeobox 2