pancreatic islet-cell hyperplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hyperplasia of the islets of Langerhans, i.e., of the regions of the pancreas that contain its endocrine cells. (Human Phenotype Ontology, HP_0004510)
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8 genes associated with the pancreatic islet-cell hyperplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
DIS3L2 DIS3 like 3'-5' exoribonuclease 2
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase)
GPC3 glypican 3
INSR insulin receptor
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
LBR lamin B receptor
SLC16A1 solute carrier family 16 (monocarboxylate transporter), member 1