hypoventilation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A reduction in the amount of air transported into the pulmonary alveoli by breathing, leading to hypercapnia (increase in the partial pressure of carbon dioxide). (Human Phenotype Ontology, HP_0002791)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002321
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Genes

4 gene mutations causing the hypoventilation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
NDN necdin, melanoma antigen (MAGE) family member
PBX3 pre-B-cell leukemia homeobox 3
PHOX2B paired-like homeobox 2b
SLC5A3 solute carrier family 5 (sodium/myo-inositol cotransporter), member 3