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GENATLAS PHENOTYPE
last update : 26-08-2019
Symbol SPGF39
Location 17q25.3
Name Spermatogenic failure 39
Corresponding gene DNAH17
Main clinical features
  • primary infertility, severe reduction of the number of spermatozoa with normal morphology compared to the normal value
  • Genetic determination
    Function/system disorder
    Type disease
    Remark(s) . mutations in DNAH17 are responsible for isolated male infertility (PMID: 31178125))