megacolon Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A colonic disease that is characterized by an abnormal dilation of the colon. (Human Disease Ontology, DOID_11372)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:11372
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Genes

23 genes associated with the disease megacolon in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
RET ret proto-oncogene 1.93435
CSGALNACT2 chondroitin sulfate N-acetylgalactosaminyltransferase 2 1.88677
RASGEF1A RasGEF domain family, member 1A 1.87206
GFRA1 GDNF family receptor alpha 1 1.83757
KIR2DS4 killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 4 1.60128
NRG1 neuregulin 1 1.39396
ABHD1 abhydrolase domain containing 1 1.29707
TACC2 transforming, acidic coiled-coil containing protein 2 1.13329
GNG4 guanine nucleotide binding protein (G protein), gamma 4 1.08934
ABLIM1 actin binding LIM protein 1 1.0549
TCERG1L transcription elongation regulator 1-like 0.953745
ANTXRL anthrax toxin receptor-like 0.922781
CAPN5 calpain 5 0.897579
ADARB2 adenosine deaminase, RNA-specific, B2 (non-functional) 0.877977
MCC mutated in colorectal cancers 0.857874
GJA8 gap junction protein, alpha 8, 50kDa 0.855811
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1 0.847035
MED20 mediator complex subunit 20 0.838994
PEBP4 phosphatidylethanolamine-binding protein 4 0.807012
CNTN4 contactin 4 0.785677
SORCS3 sortilin-related VPS10 domain containing receptor 3 0.784108
GRM8 glutamate receptor, metabotropic 8 0.77375
AUTS2 autism susceptibility candidate 2 0.671862