absent presphenoid bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the anterior part of the body of the sphenoid bone in front of the basisphenoid; it is usually a separate bone in the young or fetus, but becomes a part of the sphenoid in the adult (Mammalian Phenotype Ontology, MP_0004449)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004449
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9 gene mutations causing the absent presphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALX1 ALX homeobox 1
APAF1 apoptotic peptidase activating factor 1
FGFR2 fibroblast growth factor receptor 2
FOXC2 forkhead box C2
GLI2 GLI family zinc finger 2
IRF6 interferon regulatory factor 6
LMO4 LIM domain only 4
PTCH1 patched 1
TMEM107 transmembrane protein 107