abnormal lateral plate mesoderm morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the portion of the middle of the three primary germ layers of the embryo that resides on the periphery of the embryo, is continuous with the extra-embryonic mesoderm, splits into two layers enclosing the intra-embryonic coelom, and gives rise to body wall structures (Mammalian Phenotype Ontology, MP_0010117)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010117
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8 gene mutations causing the abnormal lateral plate mesoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP4 bone morphogenetic protein 4
CLUAP1 clusterin associated protein 1
FGFR1 fibroblast growth factor receptor 1
FN1 fibronectin 1
FOXF1 forkhead box F1
ISL1 ISL LIM homeobox 1
NODAL nodal growth differentiation factor
VPS41 vacuolar protein sorting 41 homolog (S. cerevisiae)