fusion of basioccipital and basisphenoid bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description union of the basioccipital and basisphenoid bones into one structure, when this fusion does not normally occur (such as in a species where these bones normally persist as separate entities) (Mammalian Phenotype Ontology, MP_0004572)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004572
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3 gene mutations causing the fusion of basioccipital and basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHRD chordin
FGFRL1 fibroblast growth factor receptor-like 1
TBX1 T-box 1