absent vertebral body Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the main cylindrical portion of the vertebra ventral to the vertebral canal (Mammalian Phenotype Ontology, MP_0004668)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004668
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3 gene mutations causing the absent vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
NKX3-2 NK3 homeobox 2
PAX1 paired box 1
TBX1 T-box 1