Esophageal Stenosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormal narrowing of the lumen of the esophagus. (Human Phenotype Ontology, HP_0010450)
External Link https://www.disgenet.org/browser/0/1/0/C0014866
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Genes

16 genes associated with the disease Esophageal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACD adrenocortical dysplasia homolog (mouse)
CEACAM5 carcinoembryonic antigen-related cell adhesion molecule 5
CTC1 CTS telomere maintenance complex component 1
DKC1 dyskeratosis congenita 1, dyskerin
IL6 interleukin 6
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NHP2 NHP2 ribonucleoprotein
NOP10 NOP10 ribonucleoprotein
PARN poly(A)-specific ribonuclease
RTEL1 regulator of telomere elongation helicase 1
SOD2 superoxide dismutase 2, mitochondrial
TERT telomerase reverse transcriptase
TINF2 TERF1 (TRF1)-interacting nuclear factor 2
USB1 U6 snRNA biogenesis 1
WRAP53 WD repeat containing, antisense to TP53