LRRC71

LRRC71, also known as Leucine-rich repeat-containing protein 71, is a protein that in humans is encoded by the LRRC71 gene. This gene is located on chromosome 19q13.3. LRRC71 is a member of the leucine-rich repeat-containing (LRR) family of proteins, which are characterized by the presence of multiple leucine-rich repeats in their amino acid sequences.

LRRC71 is expressed in various tissues, including the brain, heart, and kidney. Its precise function is not fully understood, but it is believed to play a role in cellular signaling and protein-protein interactions. Some studies suggest that LRRC71 may be involved in the regulation of gene expression and the maintenance of cellular homeostasis.

Mutations in the LRRC71 gene have been associated with several genetic disorders, including intellectual disability, autism spectrum disorder, and schizophrenia. However, the relationship between LRRC71 mutations and these disorders is complex and not fully understood. Further research is needed to elucidate the role of LRRC71 in these conditions and to develop potential therapeutic strategies.

LRRC71 is also a potential target for drug development, as its involvement in cellular signaling and protein-protein interactions makes it a promising candidate for the treatment of various diseases. Ongoing research is focused on understanding the molecular mechanisms underlying LRRC71 function and its role in disease pathogenesis.