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GENATLAS PHENOTYPE

last update : 22-06-2022

Symbol	SPGF69
Location	19q13.2
Name	spermatogenic failure 69
Corresponding gene	GGN
Main clinical features	infertility due to sperm being round-headed (globozoospermia) and lacking the acrosome
Genetic determination	autosomal recessive
Function/system disorder	sex-genitalia
Type	disease

Remark(s)