esophageal neoplasm Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A tumor (abnormal growth of tissue) of the esophagus. (Human Phenotype Ontology, HP_0100751)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100751
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Genes

11 genes associated with the esophageal neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASCC1 activating signal cointegrator 1 complex subunit 1
CTHRC1 collagen triple helix repeat containing 1
FH fumarate hydratase
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
MSR1 macrophage scavenger receptor 1
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
RHBDF2 rhomboid 5 homolog 2 (Drosophila)
SDHA succinate dehydrogenase complex, subunit A, flavoprotein (Fp)
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
STK11 serine/threonine kinase 11