abnormal pancreatic islet number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the number of the clusters of hormone-producing cells that are scattered throughout the pancreas (Mammalian Phenotype Ontology, MP_0009166)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009166
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21 gene mutations causing the abnormal pancreatic islet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
BAD BCL2-associated agonist of cell death
BGLAP bone gamma-carboxyglutamate (gla) protein
BRD2 bromodomain containing 2
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CPE carboxypeptidase E
CTF1 cardiotrophin 1
E2F1 E2F transcription factor 1
GCG glucagon
GDF11 growth differentiation factor 11
ICOS inducible T-cell co-stimulator
LEP leptin
NCOA5 nuclear receptor coactivator 5
PAX2 paired box 2
PDX1 pancreatic and duodenal homeobox 1
PITPNA phosphatidylinositol transfer protein, alpha
PKD1 polycystic kidney disease 1 (autosomal dominant)
SEC23B Sec23 homolog B (S. cerevisiae)
SERTAD1 SERTA domain containing 1
TK1 thymidine kinase 1, soluble
TLR3 toll-like receptor 3