abnormal styloid process morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the slender needle-like pointed projection that runs downward and slightly forward from the base of the inferior surface of the petrous portion of the temporal bone where it joins the tympanic portion; it gives attachment to the styloglossus, stylohyoid, and stylopharyngeus muscles and the stylohyoid and stylomandibular ligaments (Mammalian Phenotype Ontology, MP_0008023)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008023
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10 gene mutations causing the abnormal styloid process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DLX5 distal-less homeobox 5
ECE1 endothelin converting enzyme 1
EDNRA endothelin receptor type A
FGFR1 fibroblast growth factor receptor 1
GBX2 gastrulation brain homeobox 2
HOXA2 homeobox A2
NOG noggin
PBX1 pre-B-cell leukemia homeobox 1
POU3F3 POU class 3 homeobox 3
SIX1 SIX homeobox 1