|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 gene mutations causing the pigmented parathyroid gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.