Aliases for SYCP3 Gene
External Ids for SYCP3 Gene
Previous GeneCards Identifiers for SYCP3 Gene
This gene encodes an essential structural component of the synaptonemal complex. This complex is involved in synapsis, recombination and segregation of meiotic chromosomes. Mutations in this gene are associated with azoospermia in males and susceptibility to pregnancy loss in females. Alternate splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, May 2010]
GeneCards Summary for SYCP3 Gene
SYCP3 (Synaptonemal Complex Protein 3) is a Protein Coding gene. Diseases associated with SYCP3 include Spermatogenic Failure 4 and Azoospermia. Among its related pathways are Meiosis and Cell Cycle, Mitotic.
UniProtKB/Swiss-Prot for SYCP3 Gene
Component of the synaptonemal complexes (SCS), formed between homologous chromosomes during meiotic prophase. Required for centromere pairing during meiosis in male germ cells (By similarity). Required for normal meiosis during spermatogenesis and male fertility (PubMed:14643120). Plays a lesser role in female fertility. Required for efficient phosphorylation of HORMAD1 and HORMAD2 (By similarity).