absent reichert cartilage Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the cartilage normally found in the mesenchyme of the second branchial arch in the embryo, from which develop the stapes, the styloid processes, the stylohyoid ligaments, and the lesser cornua of the hyoid bone (Mammalian Phenotype Ontology, MP_0004916)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004916
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Genes

1 gene mutations causing the absent reichert cartilage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PAX9 paired box 9