absent basisphenoid bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the part of the base of the cranium found between the basioccipital and the presphenoid bone (Mammalian Phenotype Ontology, MP_0008385)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008385
Similar Terms
Downloads & Tools


2 gene mutations causing the absent basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DISP1 dispatched homolog 1 (Drosophila)
NKX3-2 NK3 homeobox 2