absent sternum body Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the middle and longest portion of the sternum, lying between the manubrium superiorly and the xiphoid process inferiorly; the body of the sternum (gladiolus) is considerably lengthier, narrower, and thinner than the manubrium, attaining its greatest breadth close to the lower end (Mammalian Phenotype Ontology, MP_0012513)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012513
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Genes

1 gene mutations causing the absent sternum body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXC1 forkhead box C1