decreased circulating parathyroid hormone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the blood concentration of the hormone that regulates and maintains intracellular calcium levels in the body (Mammalian Phenotype Ontology, MP_0002905)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002905
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Genes

10 gene mutations causing the decreased circulating parathyroid hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CASR calcium-sensing receptor
CLEC2D C-type lectin domain family 2, member D
CRH corticotropin releasing hormone
FGF23 fibroblast growth factor 23
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3
GCM2 glial cells missing homolog 2 (Drosophila)
GNAS GNAS complex locus
JAK1 Janus kinase 1
PTH1R parathyroid hormone 1 receptor
SLC34A1 solute carrier family 34 (type II sodium/phosphate cotransporter), member 1