absent sternum Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description missing long flat bone of the chest; articulates with clavicle and first seven rib pairs (Mammalian Phenotype Ontology, MP_0000158)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000158
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3 gene mutations causing the absent sternum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXC1 forkhead box C1
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)