decreased cranial neural crest cell number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the number of neural crest cells (NCCs) originating in the anterior part of the developing embryo and residing between the mid-diencephalon and the forming hindbrain; cranial NCCs migrate dorsolaterally to form the craniofacial mesenchyme that differentiates into various craniofacial cartilages and bones, cranial neurons, glia, and connective tissues of the face; these cells enter the pharyngeal pouches and arches where they give rise to thymic cells, bones of the middle ear and jaw (mandible), and the odontoblasts of the tooth primordial; like their counterparts in the trunk, cranial NCCs also contribute to the developing peripheral nervous system, along with the pigmented cell (i.e. melanocyte) lineage (Mammalian Phenotype Ontology, MP_0012755)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012755
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Genes

1 gene mutations causing the decreased cranial neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EFNB2 ephrin-B2