abnormal circulating ghrelin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the blood concentration of the peptide hormone produced mainly by P/D1 cells lining the fundus of the stomach and epsilon cells of the pancreas that stimulates hunger and serves as a potent stimulator of growth hormone from the anterior pituitary gland; in addition to stimulating appetite and growth, ghrelin also plays various roles in energy homeostasis, neuropathy, and in the cardiovascular and immune systems (Mammalian Phenotype Ontology, MP_0011611)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011611
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Genes

7 gene mutations causing the abnormal circulating ghrelin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CORT cortistatin
CSHL1 chorionic somatomammotropin hormone-like 1
GNAS GNAS complex locus
GPR26 G protein-coupled receptor 26
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
MBOAT4 membrane bound O-acyltransferase domain containing 4
SST somatostatin