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OMIM

Gene

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GENATLAS PHENOTYPE

last update : 29/09/2008

Symbol	TBG
Location	Xq22.2
Name	thyroxine-binding globulin deficiency
Corresponding gene	SERPINA7
Main clinical features	hyperthyroxinemia, euthyroidal, with reduced or increased thyroxine-binding globulin and, reduced or elevated protein-bound iodine (PBI)
Genetic determination	sex linked
Function/system disorder	endocrinology
Type	disease

Gene product

Name	thyroxin binding globulin (SERPINA7)

Remark(s)