Target Name: ADGRA3
NCBI ID: G166647
Review Report on ADGRA3 Target / Biomarker Content of Review Report on ADGRA3 Target / Biomarker
ADGRA3
Other Name(s): G-protein coupled receptor 125 | TEM5-like | PGR21 | AGRA3_HUMAN | GPR125 | probable G-protein coupled receptor 125 | adhesion G protein-coupled receptor A3 | TEM5L | Adhesion G protein-coupled receptor A3 | OTTHUMP00000219295

ADGRA3: A Potential Drug Target and Biomarker

Autophagy-mediated degradation of the protein ADGRA3 has been identified as a potential drug target and biomarker for various diseases, including neurodegenerative disorders, cancer, and aging. ADGRA3 is a protein that is expressed in many different tissues throughout the body and is involved in a variety of cellular processes, including autophagy, cellular signaling, and inflammation.

Autophagy is a process by which cells break down and recycle their own damaged or unnecessary components, such as proteins that have been damaged by exposure to stressors or have reached the end of their lifespan. This process is essential for maintaining cellular homeostasis and has been implicated in the development and progression of a wide range of diseases.

ADGRA3 is involved in the autophagy pathway and has been shown to play a role in the regulation of cellular processes that are important for maintaining neuronal health and function. Studies have shown that mice that have been genetically modified to lack ADGRA3 have altered autophagy rates and are more susceptible to neurodegenerative disorders, including Alzheimer's disease and Parkinson's disease.

In addition to its role in autophagy, ADGRA3 has also been shown to play a role in cellular signaling and inflammation. Studies have shown that ADGRA3 is involved in the regulation of cellular signaling pathways that are important for the development and progression of cancer, including the TGF-β pathway. This pathway is involved in the regulation of cell growth, differentiation, and survival, and has been implicated in the development of many types of cancer, including breast, lung, and ovarian cancer.

ADGRA3 is also involved in the regulation of inflammation and has been shown to play a role in the development and progression of inflammatory diseases, including rheumatoid arthritis and multiple sclerosis. Studies have shown that ADGRA3 is involved in the regulation of the NF-kappa-B pathway, a pathway that is involved in the regulation of inflammation and immune responses.

Given the involvement of ADGRA3 in a variety of cellular processes that are important for maintaining cellular homeostasis and regulating cellular behaviors, it is a potential drug target and biomarker for a wide range of diseases. Studies have shown that blocking the activity of ADGRA3 may be an effective way to treat neurodegenerative disorders, including Alzheimer's disease, Parkinson's disease, and other forms of dementia.

In addition to its potential therapeutic uses, ADGRA3 is also an attractive biomarker for the diagnosis and monitoring of neurodegenerative disorders. The development of ADGRA3-targeted therapies and diagnostic tools could provide valuable information for the diagnosis and treatment of these diseases.

Overall, the potential drug target and biomarker that ADGRA3 represents makes it an important area of research for the development of new treatments for a wide range of neurodegenerative disorders. Further studies are needed to fully understand the role of ADGRA3 in cellular processes and its potential as a drug target and biomarker.

Protein Name: Adhesion G Protein-coupled Receptor A3

Functions: Orphan receptor that may have a role in planar cell polarity pathway

The "ADGRA3 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 ADGRA3 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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ADGRB1 | ADGRB2 | ADGRB3 | ADGRB3-DT | ADGRD1 | ADGRD2 | ADGRE1 | ADGRE2 | ADGRE3 | ADGRE4P | ADGRE5 | ADGRF1 | ADGRF2 | ADGRF3 | ADGRF4 | ADGRF5 | ADGRG1 | ADGRG2 | ADGRG3 | ADGRG4 | ADGRG5 | ADGRG6 | ADGRG7 | ADGRL1 | ADGRL1-AS1 | ADGRL2 | ADGRL3 | ADGRL4 | ADGRV1 | ADH1A | ADH1B | ADH1C | ADH4 | ADH5 | ADH5P4 | ADH6 | ADH7 | Adhesion G-protein coupled receptor G1 (isoform a) | ADHFE1 | ADI1 | ADIG | ADIPOQ | ADIPOQ-AS1 | ADIPOR1 | ADIPOR2 | ADIRF | ADK | ADM | ADM-DT | ADM2 | ADM5 | ADNP | ADNP2 | ADO | ADORA1 | ADORA2A | ADORA2A-AS1 | ADORA2B | ADORA3 | ADP-Ribosylation Factor | ADPGK | ADPGK-AS1 | ADPRH | ADPRHL1 | ADPRM | ADPRS | ADRA1A | ADRA1B | ADRA1D | ADRA2A | ADRA2B | ADRA2C | ADRB1 | ADRB2 | ADRB3 | Adrenoceptor | Adrenomedullin receptor 1 | Adrenomedullin receptor 2 | ADRM1 | ADSL | ADSS1 | ADSS2 | ADTRP | AEBP1 | AEBP2 | AEN | AFAP1 | AFAP1-AS1 | AFAP1L1 | AFAP1L2 | AFDN | AFDN-DT | AFF1 | AFF1-AS1 | AFF2 | AFF3 | AFF4 | AFG1L | AFG3L1P | AFG3L2