iodide oxidation defect Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description thyroid defect in oxidation and organification of iodide (Mammalian Phenotype Ontology, MP_0003501)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003501
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Genes

1 gene mutations causing the iodide oxidation defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
TSHR thyroid stimulating hormone receptor