LRRC23

LRRC23 is a human gene that encodes for a protein of unknown function belonging to the leucine-rich repeat (LRR) superfamily.

Gene Information:

The LRRC23 gene is located on chromosome 6q25.3 in humans. It is approximately [This information should be verified with a reliable source, such as NCBI Gene or Ensembl, and the approximate size included here]. The gene contains multiple exons. Alternative splicing may result in multiple transcript variants, although their precise functions may not be fully elucidated.

Protein Information:

The protein encoded by the LRRC23 gene is predicted to contain leucine-rich repeats, which are characteristic of proteins involved in protein-protein interactions. Proteins with LRR domains are often involved in diverse cellular processes, including signal transduction, immune response, and cell adhesion. The exact function of LRRC23 protein remains largely unknown. However, based on its structural features, it is hypothesized to interact with other proteins and potentially play a role in cellular signaling or other cellular processes. Further research is needed to determine its specific function and interacting partners. [Molecular weight information should be obtained from UniProt or similar databases and included here once found].

Expression:

Expression studies indicate that LRRC23 is expressed in various tissues. [Specific information on tissue expression patterns should be sourced from databases like GTEx or similar resources. Include information about tissues where the gene is highly expressed and tissues where expression is low or absent, if available.].

Clinical Significance:

Currently, there is limited information on the clinical significance of LRRC23. No direct association between mutations in LRRC23 and specific human diseases has been definitively established. However, given its potential role in protein-protein interactions and cellular processes, future research may uncover its involvement in disease pathogenesis. Additional studies, including genome-wide association studies (GWAS) and functional analyses, are needed to explore potential links between LRRC23 variations and human health.

Further Research:

Ongoing research efforts aim to elucidate the specific function of LRRC23 and its role in cellular processes. Future studies may focus on identifying interacting partners, investigating the effects of LRRC23 knockdown or overexpression, and examining the potential involvement of LRRC23 in disease development.