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)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0004510
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Genes

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