abnormal pharyngeal arch mesenchyme morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the primordial embryonic connective tissue associated with the branchial arches, consisting of mesenchymal cells supported in interlaminar jelly, that derive mostly from the mesoderm and contribute to facial and cranial nerve-associated structures (Mammalian Phenotype Ontology, MP_0011262)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011262
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2 gene mutations causing the abnormal pharyngeal arch mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PRDM1 PR domain containing 1, with ZNF domain
RSPO2 R-spondin 2