abnormal pre-botzinger complex physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the group of interneurons within the medulla oblongata's ventral respiratory group that are important for the generation of ventilatory (inspiratory) rhythmogenesis (Mammalian Phenotype Ontology, MP_0010746)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010746
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6 gene mutations causing the abnormal pre-botzinger complex physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DBX1 developing brain homeobox 1
KDM6B lysine (K)-specific demethylase 6B
NDN necdin, melanoma antigen (MAGE) family member
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
ROBO3 roundabout, axon guidance receptor, homolog 3 (Drosophila)
SLC17A6 solute carrier family 17 (vesicular glutamate transporter), member 6