Target Name: RXFP4
NCBI ID: G339403
Review Report on RXFP4 Target / Biomarker Content of Review Report on RXFP4 Target / Biomarker
RXFP4
Other Name(s): insulin-like peptide INSL5 receptor | RLN3R2 | G protein-coupled receptor 100 | relaxin/insulin like family peptide receptor 4 | relaxin family peptide/INSL5 receptor 4 | Relaxin 3 receptor 2 | GPCR142 | RLN3 receptor 2 | Relaxin-3 receptor 2 | G-protein coupled receptor 100 | Relaxin family peptide/INSL5 receptor 4 | RXFPR4 | MGC126558 | relaxin family peptide receptor 4 | MGC126556 | RL3R2_HUMAN | G-protein coupled receptor GPCR142 | Relaxin family peptide receptor 4 | Insulin-like peptide INSL5 receptor | GPR100

INSL5 as A Potential Drug Target and Biomarker for Type 1 Diabetes

The INSL5 receptor is a protein that is expressed in the pancreatic beta cells, which are responsible for producing insulin. Insulin is a critical hormone that regulates blood sugar levels, and beta cells are the only cells in the body that produce it. INSL5 is a protein that is expressed in the pancreatic beta cells and is involved in the production of insulin.

Recent studies have identified INSL5 as a potential drug target and biomarker for various diseases, including type 1 diabetes. INSL5 has also been shown to play a role in the development and progression of cancer.

Drug Targeting

INSL5 has been identified as a potential drug target for the treatment of type 1 diabetes. Type 1 diabetes is a chronic autoimmune disease that results in the destruction of the beta cells in the pancreatic endocrine system. The destruction of beta cells leads to a lack of insulin production, which can lead to high blood sugar levels.

One of the mechanisms by which INSL5 may contribute to the development and progression of type 1 diabetes is through its role in the regulation of immune cells. INSL5 has been shown to regulate the movement of immune cells into the pancreatic beta cells, which may play a role in the destruction of beta cells.

Another potential mechanism by which INSL5 may contribute to the development and progression of type 1 diabetes is through its role in the regulation of inflammation. INSL5 has been shown to regulate the production of pro-inflammatory cytokines, which may contribute to the development of inflammation in the pancreatic beta cells.

Biomarker

INSL5 has also been identified as a potential biomarker for the diagnosis and monitoring of type 1 diabetes. The destruction of beta cells in the pancreatic endocrine system is a hallmark feature of type 1 diabetes, and has been shown to be associated with an increased risk of complications.

Monitoring INSL5 levels in the pancreatic beta cells may be an effective way to diagnose and monitor the progression of type 1 diabetes. This could be done by measuring the levels of INSL5 in the pancreatic beta cells, as well as the levels of other proteins that are involved in the production of insulin.

Conclusion

INSL5 is a protein that is expressed in the pancreatic beta cells and is involved in the production of insulin. Recent studies have identified INSL5 as a potential drug target and biomarker for various diseases, including type 1 diabetes. The destruction of beta cells in the pancreatic endocrine system is a hallmark feature of type 1 diabetes, and has been shown to be associated with an increased risk of complications. Monitoring INSL5 levels in the pancreatic beta cells may be an effective way to diagnose and monitor the progression of type 1 diabetes. Further research is needed to fully understand the role of INSL5 in the development and progression of type 1 diabetes.

Protein Name: Relaxin Family Peptide/INSL5 Receptor 4

Functions: High affinity receptor for INSL5. Also acts as receptor for RLN3/relaxin-3, as well as bradykinin and kallidin. Binding of the ligand inhibit cAMP accumulation

The "RXFP4 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about RXFP4 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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