decreased axial mesoderm size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size or deficiency of the part of the middle of the three primary germ layers of the embryo which includes the prechordal mesoderm and the chordamesoderm and gives rise to the prechordal plate and to the notochord (Mammalian Phenotype Ontology, MP_0012272)
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3 gene mutations causing the decreased axial mesoderm size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EPB41L5 erythrocyte membrane protein band 4.1 like 5
PITX2 paired-like homeodomain 2
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha