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GENATLAS PHENOTYPE

last update : 18/10/2005

Symbol	IGHG2
Location	14q32-q33
Name	IGG2 deficiency
Corresponding gene	IGHG2
Other symbol(s)	IGG2
Main clinical features	caused by a mutated membrane-bound form of gamma 2 heavy chain, with recurrent sino-pulmonary infections
Genetic determination
Function/system disorder	hematology
Type	disease

Gene product

Name	immunoglobulin gamma 2 (IGHG2)