abnormality of endocrine pancreas physiology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A function abnormality of the endocrine pancreas. (Human Phenotype Ontology, HP_0012093)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012093
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14 genes associated with the abnormality of endocrine pancreas physiology 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
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase)
GCK glucokinase (hexokinase 4)
GPC3 glypican 3
INS insulin
INSR insulin receptor
ITS Insulinoma tumor suppressor gene locus
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
LBR lamin B receptor
MEN1 multiple endocrine neoplasia I
PAX4 paired box 4
SLC16A1 solute carrier family 16 (monocarboxylate transporter), member 1