pigmented parathyroid gland Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description presence of melanocytes and/or melanin in either of the two small, paired endocrine glands, usually found embedded in the connective tissue capsule on the posterior surface of the thyroid gland; they secrete parathyroid hormone (PTH) that regulates calcium and phosphorous metabolism (Mammalian Phenotype Ontology, MP_0003114)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003114
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Genes

1 gene mutations causing the pigmented parathyroid gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CASR calcium-sensing receptor