|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
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3 gene mutations causing the abnormal circulating pancreatic peptide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.