Central Apnea Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Apnea resulting from depression of the respiratory centers in the medulla oblongata. There is a lack of respiratory effort rather than obstruction of airflow. (Human Phenotype Ontology, HP_0002871)
External Link https://www.disgenet.org/browser/0/1/0/C3887548
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Genes

8 genes associated with the disease Central Apnea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BDNF brain-derived neurotrophic factor
MTOR mechanistic target of rapamycin (serine/threonine kinase)
PHOX2B paired-like homeobox 2b
PLCB4 phospholipase C, beta 4
REM1 RAS (RAD and GEM)-like GTP-binding 1
SLC5A3 solute carrier family 5 (sodium/myo-inositol cotransporter), member 3
TRPV1 transient receptor potential cation channel, subfamily V, member 1
UNC80 unc-80 homolog (C. elegans)