Esophageal Stricture Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A pathological narrowing of the esophagus that is caused by the development of a ring of scar tissue that constricts the esophageal lumen. (Human Phenotype Ontology, HP_0002043)
External Link https://www.disgenet.org/browser/0/1/0/C4551650
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Genes

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

Symbol Name
AAAS achalasia, adrenocortical insufficiency, alacrimia
CEACAM5 carcinoembryonic antigen-related cell adhesion molecule 5
CHST15 carbohydrate (N-acetylgalactosamine 4-sulfate 6-O) sulfotransferase 15
COL7A1 collagen, type VII, alpha 1
DKC1 dyskeratosis congenita 1, dyskerin
FERMT1 fermitin family member 1
HLA-B major histocompatibility complex, class I, B
IKZF1 IKAROS family zinc finger 1 (Ikaros)
IL6 interleukin 6
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
LAMA3 laminin, alpha 3
LAMB3 laminin, beta 3
LAMC2 laminin, gamma 2
MMP1 matrix metallopeptidase 1
NHP2 NHP2 ribonucleoprotein
NOP10 NOP10 ribonucleoprotein
SOD2 superoxide dismutase 2, mitochondrial
TERT telomerase reverse transcriptase
TMSB4X thymosin beta 4, X-linked