CATSPER2, a human autosomal nonsyndromic male infertility gene

Eur J Hum Genet. 2003 Jul;11(7):497-502. doi: 10.1038/sj.ejhg.5200991.


In the course of positional cloning of the Congenital Dyserythropoietic Anemia type I (CDAI) [MIM 224120] gene on 15q15.1-15.3, we examined a family of French origin, in which the propositus suffered from asthenoteratozoospermia and nonsyndromic deafness in addition to CDAI. Two of his brothers had a similar phenotype. All three siblings were homozygous carriers of the CDA1 mutation as well as of a distally located approximately 70 kb deletion of the proximal copy of a 106 kb tandem repeat on chromosome 15q15. These repeats encode four genes whose distal copies may be considered pseudogenes. Lack of functional stereocilin and CATSPER2 (a voltage-gate cation channel expressed specifically in spermatozoa) may explain the observed deafness and male infertility phenotypes. To the best of our knowledge, the involvement of CATSPER2 in asthenoteratozoospermia is the first description of a human autosomal gene defect associated with nonsyndromic male infertility.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anemia, Dyserythropoietic, Congenital / genetics*
  • Calcium Channels / genetics*
  • Chromosomes, Human, Pair 15
  • Deafness / genetics*
  • Female
  • Humans
  • Infertility, Male / genetics*
  • Ion Channels / genetics*
  • Male
  • Pedigree
  • Phenotype
  • Seminal Plasma Proteins / genetics*
  • Sequence Deletion


  • CATSPER2 protein, human
  • Calcium Channels
  • CatSper2 protein, mouse
  • Ion Channels
  • Seminal Plasma Proteins