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GENATLAS PHENOTYPE

last update : 23-03-2021

Symbol	SPGF32
Location	9q34.3
Name	spermatogenic failure 32
Corresponding gene	SOHLH1
Main clinical features	male infertility due to nonobstructive azoospermia testicular biopsy has shown absence of spermatogenic cells and a Sertoli cell-only pattern
Genetic determination	autosomal dominant
Function/system disorder	sex-genitalia
Type	disease

Remark(s)