|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 gene mutations causing the abnormal retrotrapezoid nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|PHOX2B||paired-like homeobox 2b|