Secretory Diarrhea Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Secretory diarrhea is a diarrhea where there is an increase in the active secretion, or there is an inhibition of absorption causing little to no structural damage. The most common cause of this type of diarrhea is a cholera toxin that stimulates the secretion of anions, especially chloride ions. (Human Disease Ontology, DOID_0050129)
External Link	https://www.disgenet.org/browser/0/1/0/C0267557
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Genes

18 genes associated with the disease Secretory Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ABCC4	ATP-binding cassette, sub-family C (CFTR/MRP), member 4
ANO6	anoctamin 6
CFTR	cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
FOXP3	forkhead box P3
GUCA2A	guanylate cyclase activator 2A (guanylin)
GUCA2B	guanylate cyclase activator 2B (uroguanylin)
IL13RA1	interleukin 13 receptor, alpha 1
MYO5B	myosin VB
NLRC4	NLR family, CARD domain containing 4
PLVAP	plasmalemma vesicle associated protein
RAC2	ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2)
SLC26A3	solute carrier family 26 (anion exchanger), member 3
SLC5A1	solute carrier family 5 (sodium/glucose cotransporter), member 1
SLC9A3	solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
SLC9A3R2	solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 2
SPINT2	serine peptidase inhibitor, Kunitz type, 2
TAPBP	TAP binding protein (tapasin)
VIP	vasoactive intestinal peptide