pancreatic islet hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description overdevelopment or increased size of the clusters of hormone-producing cells that are scattered throughout the pancreas, usually due an increased number of cells (Mammalian Phenotype Ontology, MP_0005491)
External Link
Similar Terms
Downloads & Tools


29 gene mutations causing the pancreatic islet hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALMS1 Alstrom syndrome protein 1
ANXA7 annexin A7
ATXN2 ataxin 2
BRD2 bromodomain containing 2
CCDC80 coiled-coil domain containing 80
CPE carboxypeptidase E
EHD4 EH-domain containing 4
GCGR glucagon receptor
GDF11 growth differentiation factor 11
INVS inversin
LEP leptin
LEPR leptin receptor
LIPE lipase, hormone-sensitive
MEN1 multiple endocrine neoplasia I
PAX2 paired box 2
PDPK1 3-phosphoinositide dependent protein kinase 1
PGR progesterone receptor
PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta
PPARG peroxisome proliferator-activated receptor gamma
PRKCI protein kinase C, iota
RAPGEF3 Rap guanine nucleotide exchange factor (GEF) 3
RIMS2 regulating synaptic membrane exocytosis 2
SCG5 secretogranin V
SH2B1 SH2B adaptor protein 1
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4
SOX9 SRY (sex determining region Y)-box 9
THBS1 thrombospondin 1
TNK1 tyrosine kinase, non-receptor, 1
TOP3B topoisomerase (DNA) III beta