Meconium Ileus Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Obstruction of the intestine due to abnormally thick meconium. (Human Phenotype Ontology, HP_0004401)
External Link https://www.disgenet.org/browser/0/1/0/C2939175
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Genes

22 genes associated with the disease Meconium Ileus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADIPOR2 adiponectin receptor 2
AFP alpha-fetoprotein
ATP12A ATPase, H+/K+ transporting, nongastric, alpha polypeptide
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CLCA1 chloride channel accessory 1
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
FEV FEV (ETS oncogene family)
GOT2 glutamic-oxaloacetic transaminase 2, mitochondrial
GUCA2A guanylate cyclase activator 2A (guanylin)
GUCY2C guanylate cyclase 2C
HFE hemochromatosis
MSRA methionine sulfoxide reductase A
MUC1 mucin 1, cell surface associated
MUC2 mucin 2, oligomeric mucus/gel-forming
MUC5AC mucin 5AC, oligomeric mucus/gel-forming
PRSS1 protease, serine, 1 (trypsin 1)
SLC1A5 solute carrier family 1 (neutral amino acid transporter), member 5
SLC26A9 solute carrier family 26 (anion exchanger), member 9
SLC6A14 solute carrier family 6 (amino acid transporter), member 14
SLC9A3 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
TGFB1 transforming growth factor, beta 1
TRIP12 thyroid hormone receptor interactor 12