abnormal retrotrapezoid nucleus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the loose collection of neurons that reside in the rostral medulla close to the medullary surface, ventral and immediately caudal of nVII, that are crucial for CO2 sensing in the brain (Mammalian Phenotype Ontology, MP_0011406)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011406
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Genes

1 gene mutations causing the abnormal retrotrapezoid nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PHOX2B paired-like homeobox 2b