Aliases for VCY1B Gene
External Ids for VCY1B Gene
Previous GeneCards Identifiers for VCY1B Gene
The protein encoded by this gene is a member of a family of human VCX/Y genes. This gene family has multiple members on both X and Y chromosomes, and all are expressed exclusively in male germ cells. Members of the VCX/Y family share a high degree of sequence identity, with the exception that a 30-bp unit is tandemly repeated in X-linked members but occurs only once in Y-linked members. VCX/Y genes encode small and highly charged proteins of unknown function. This gene encodes a small, positively charged protein. The presence of a putative bipartite nuclear localization signal suggests that this gene encodes a nuclear protein. The genome has two identical copies of this gene within a palindromic region; this record represents the more telomeric copy. [provided by RefSeq, Jul 2008]
GeneCards Summary for VCY1B Gene
VCY1B (Variable Charge, Y-Linked 1B) is a Protein Coding gene. Diseases associated with VCY1B include Chronic Laryngitis and Non-Syndromic X-Linked Intellectual Disability. An important paralog of this gene is VCY.
UniProtKB/Swiss-Prot for VCY1B Gene
May mediate a process in spermatogenesis or may play a role in sex ratio distortion.