abnormal oropharynx morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the portion of the pharynx that lies between the soft palate and the upper edge of the epiglottis (Mammalian Phenotype Ontology, MP_0002252)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002252
Similar Terms
Downloads & Tools


5 gene mutations causing the abnormal oropharynx morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHRD chordin
LAMB3 laminin, beta 3
NKX2-3 NK2 homeobox 3
PGAP1 post-GPI attachment to proteins 1
TWSG1 twisted gastrulation BMP signaling modulator 1