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GENATLAS PHENOTYPE
last update : 30-09-2020
Symbol SPGF36
Location 14q13.2
Name spermatogenic failure 36
Corresponding gene PPP2R3C
Main clinical features
  • characterized by reduced fertility due to teratozoospermia, with spermatozoa showing anomalies of the head, acrosome, and nucleus
  • Genetic determination autosomal dominant
    Function/system disorder
    Type disease
    Remark(s)