abnormal circulating pancreatic peptide level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the amount of the 36-amino acid pancreatic hormone in the blood that is secreted mainly by endocrine cells found at the periphery of the islets of Langerhans in response to ingestions, and regulates gastric secretion, gastric emptying, pancreatic enzyme secretion, and appetite (Mammalian Phenotype Ontology, MP_0008459)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008459
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Genes

3 gene mutations causing the abnormal circulating pancreatic peptide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
LEP leptin
NPY2R neuropeptide Y receptor Y2
NPY4R neuropeptide Y receptor Y4