abnormal pharynx morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the passage between the mouth and the posterior nares and the larynx and esophagus (Mammalian Phenotype Ontology, MP_0002234)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002234
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12 gene mutations causing the abnormal pharynx morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHRD chordin
DISP1 dispatched homolog 1 (Drosophila)
LAMB3 laminin, beta 3
NKX2-3 NK2 homeobox 3
NKX2-5 NK2 homeobox 5
OTX2 orthodenticle homeobox 2
PGAP1 post-GPI attachment to proteins 1
SFN stratifin
SHH sonic hedgehog
SIM2 single-minded family bHLH transcription factor 2
TBX1 T-box 1
TWSG1 twisted gastrulation BMP signaling modulator 1