PRR23C

PRR23C is a human gene that encodes a protein of unknown function. The gene is located on chromosome 11 at position 11p15.5. Little is currently known about the precise role of the PRR23C protein, however, bioinformatics analysis suggests it contains a proline-rich region, which is a common motif in proteins involved in signal transduction and protein-protein interactions.

Due to the limited research available, the specific tissues and cell types where PRR23C is expressed, its interacting partners, and its involvement in any biological pathways are largely uncharacterized. Expression data, where available, hints at potential expression in various tissues, but further experimental validation is required to confirm these findings.

The PRR23C gene has been identified in genomic studies, and variations in the gene sequence have been noted. However, the association of these variations with any specific diseases or phenotypic traits is currently unclear and requires further investigation. Further research is needed to elucidate the function of PRR23C and its potential role in human health and disease.