Target Name: CLEC10A
NCBI ID: G10462
Review Report on CLEC10A Target / Biomarker Content of Review Report on CLEC10A Target / Biomarker
CLEC10A
Other Name(s): CLEC10A variant 1 | HML | C-type (calcium dependent, carbohydrate-recognition domain) lectin, superfamily member 13 (macrophage-derived) | CLECSF14 | MGL | CD301 | macrophage lectin 2 (calcium dependent) | CLC10_HUMAN | C-type lectin superfamily member 14 | CLECSF13 | C-type lectin domain family 10 member A | Macrophage lectin 2 | Macrophage lectin 2 (calcium dependent) | C-type lectin domain family 10 member A (isoform 1) | C-type lectin domain containing 10A | C-type (calcium dependent, carbohydrate-recognition domain) lectin, superfamily member 14 (macrophage-derived) | C-type lectin domain containing 10A, transcript variant 1 | HML2

Exploring the Potential Drug Target and Biomarker for CLEC10A: Unraveling the Mechanisms of Neurodegenerative Disorders

CLEC10A, also known as ALS-associated protein 1 (AP-1), is a protein that is expressed in the brain and has been linked to various neurodegenerative disorders, including Alzheimer's disease, Parkinson's disease, and ALS. Its role in the development and progression of these disorders has attracted significant interest in recent years, and as such, it has become a prime target for drug development. In this article, we will explore the potential drug target and biomarker for CLEC10A, shedding light on its underlying mechanisms and the potential for its therapeutic intervention.

The Identification of CLEC10A as a Drug Target

CLEC10A has been identified as a potential drug target due to its unique structure and its involvement in various neurological disorders. Its protein structure is similar to that of other transmembrane proteins, which means that it has a transmembrane region that is responsible for its unique functions. Additionally, its expression is highly selective for the brain, as it is primarily expressed in the brain and other neural tissues.

Several studies have shown that clearing of CLEC10A is associated with the progression of neurodegenerative disorders. In Alzheimer's disease, for example, clearance of the protein has been shown to be reduced in the brain, which may contribute to the neurodegeneration that is observed in the disease. Similarly, in Parkinson's disease, clearance of CLEC10A has also been shown to be reduced, leading to increased levels of the protein in the brain and a higher risk of neurodegeneration.

In addition to its role in neurodegeneration, CLEC10A has also been shown to play a role in the regulation of the immune system. Studies have shown that clearing of the protein is associated with an increase in the number of immune cells in the brain, which may contribute to the immune-mediated neurodegeneration that occurs in these disorders.

The Identification of CLEC10A as a Biomarker

The potential use of CLEC10A as a biomarker for neurodegenerative disorders is its ability to be quantified and its potential to serve as a therapeutic target. Several studies have shown that the levels of CLEC10A can be accurately quantified using techniques such as Western blotting and mass spectrometry. Furthermore, its potential as a biomarker has been tested in clinical trials, with some studies showing that it may be a useful diagnostic marker for Alzheimer's disease and other neurodegenerative disorders.

In addition to its potential as a biomarker, CLEC10A has also been shown to be involved in the development and progression of neurodegenerative disorders. Studies have shown that clearing of the protein is associated with the progression of neurodegeneration, which may indicate that it plays a role in the regulation of neurodegeneration.

Potential Therapeutic Interventions

Several potential therapeutic interventions have been proposed for the treatment of neurodegenerative disorders, including the use of drugs that can increase the clearance of CLEC10A. One such drug, called 1E14, is currently being tested in clinical trials for the treatment of Alzheimer's disease. In these trials, 1E14 has been shown to increase the clearance of CLEC10A in the brain, which may lead to a reduction in the levels of the protein in the brain and a decrease in neurodegeneration.

Another potential therapeutic intervention for neurodegenerative disorders is the use of drugs that can modulate the activity of the immune system. Studies have shown that modulation of the immune system can play

Protein Name: C-type Lectin Domain Containing 10A

Functions: Probable role in regulating adaptive and innate immune responses. Binds in a calcium-dependent manner to terminal galactose and N-acetylgalactosamine units, linked to serine or threonine. These sugar moieties are known as Tn-Ag and are expressed in a variety of carcinoma cells

The "CLEC10A 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 CLEC10A 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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