aplasia/hypoplasia of the pancreas Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congential underdevelopment (aplasia or hypoplasia) of the pancreas. (Human Phenotype Ontology, HP_0100800)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100800
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Genes

7 genes associated with the aplasia/hypoplasia of the pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
GATA6 GATA binding protein 6
HNF1B HNF1 homeobox B
LHX1 LIM homeobox 1
PDX1 pancreatic and duodenal homeobox 1
RARB retinoic acid receptor, beta
STRA6 stimulated by retinoic acid 6