abnormal primary palate development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the formation of the part of the shelf separating the oral and nasal cavities that is formed during early embryonic development from the medial nasal processes which derive from the frontonasal process; these merge with each other and with the bilateral maxillary processes to form the upper lip and the primary palate (Mammalian Phenotype Ontology, MP_0009654)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009654
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Genes

1 gene mutations causing the abnormal primary palate development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDON cell adhesion associated, oncogene regulated