LHFPL5

LHFPL5 is a human gene that encodes a protein of unknown function. The gene is located on chromosome 6 at position 6q14.1.

Gene Information

• Symbol: LHFPL5
• Full Name: Lipoma HMGIC fusion partner-like 5
• Location: Chromosome 6q14.1

Protein Information

The LHFPL5 gene encodes a protein, but its precise function remains largely unclear. The protein belongs to the LHFPL family of proteins, which are thought to be involved in various cellular processes, potentially related to cell adhesion, migration, or signal transduction. However, there is limited experimental evidence to confirm the exact role of LHFPL5.

Expression

Expression data for LHFPL5 indicates that it is expressed in various tissues, including brain and testes. However, the specific expression pattern and its regulation are not fully understood. Further research is needed to determine when and where the LHFPL5 gene is active during development and in adult tissues.

Clinical Significance

Currently, there are no strong associations between LHFPL5 mutations and specific diseases or disorders. However, given its location on chromosome 6 and potential role in cell function, further research may reveal its involvement in certain genetic conditions. Studies exploring the relationship between LHFPL5 and diseases are ongoing.

Further Research

Further research is required to elucidate the precise function of the LHFPL5 protein, its role in cellular processes, and its potential involvement in human diseases. Studies focusing on protein-protein interactions, cellular localization, and functional assays are needed to gain a better understanding of this gene.