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GENATLAS PHENOTYPE

last update : 7/11/2005

Symbol	SLC5A5
Location	19p13.2-p12
Name	thyroid hormonogenesis, genetic defect in, I
Other name(s)	iodine accumulation, transport or trapping defect
Corresponding gene	SLC5A5
Main clinical features	congenital hypothyroidism with goiter, low thyroidal and salivary gland radioiodide uptake
Genetic determination
Function/system disorder	endocrinology
Type	disease

Gene product

Name	solute carrier family 5 member 5, sodium-iodide symporter SLC5A5