Target Name: MOSPD1
NCBI ID: G56180
Review Report on MOSPD1 Target / Biomarker Content of Review Report on MOSPD1 Target / Biomarker
MOSPD1
Other Name(s): MOSPD1 variant 1 | Motile sperm domain-containing protein 1 (isoform 1) | MSPD1_HUMAN | DJ473B4 | motile sperm domain containing 1 | Motile sperm domain-containing protein 1 | Motile sperm domain containing 1, transcript variant 1

MOSPD1: Potential Drug Target Or Biomarker for Various Diseases

MOSPD1 (MOSPD1 variant 1) is a protein that is expressed in various tissues of the body, including the brain, pancreas, and muscle. It is a member of the MOSP family of proteins, which are known for their role in intracellular signaling.

MOSPD1 has been identified as a potential drug target or biomarker for various diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. This is because it is involved in a variety of cellular processes that are important for normal tissue function, and abnormalities in these processes can contribute to the development and progression of these diseases.

One of the key functions of MOSPD1 is its role in intracellular signaling. It is a negative regulator of the protein kinase A尾4, which is involved in the formation of beta-amyloid plaques, a hallmark of Alzheimer's disease. MOSPD1 has been shown to interact with A尾4 and to regulate its activity. This interaction between MOSPD1 and A尾4 suggests that MOSPD1 may be a useful target for drugs that are designed to inhibit the formation of beta-amyloid plaques.

In addition to its role in intracellular signaling, MOSPD1 is also involved in the regulation of cellular processes that are important for tissue repair and regeneration. It is a factor that is involved in the formation of new blood vessels in response to injury or inflammation . This suggests that MOSPD1 may be a useful target for drugs that are designed to stimulate tissue repair and regeneration.

MOSPD1 has also been shown to be involved in the regulation of cell adhesion. It is a member of the cadherin family of proteins, which are involved in cell-cell adhesion. MOSPD1 has also been shown to interact with the protein E-cadherin, which is involved in the formation of tight junctions, a type of cell-cell adhesion. This interaction between MOSPD1 and E-cadherin suggests that MOSPD1 may be a useful target for drugs that are designed to inhibit cell-cell adhesion.

In conclusion, MOSPD1 is a protein that is involved in a variety of cellular processes that are important for normal tissue function. It is a negative regulator of the protein kinase A尾4, which is involved in the formation of beta-amyloid plaques, a hallmark of Alzheimer's disease. It is also involved in the regulation of intracellular signaling, cell adhesion, and tissue repair and regeneration. As a result, MOSPD1 is a potential drug target or biomarker for a variety of diseases, including cancer, neurodegenerative diseases, and autoimmune disorders .

Protein Name: Motile Sperm Domain Containing 1

Functions: Plays a role in differentiation and/or proliferation of mesenchymal stem cells. Proposed to be involved in epithelial-to-mesenchymal transition (EMT). However, another study suggests that it is not required for EMT or stem cell self-renewal and acts during later stages of differentiation

The "MOSPD1 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 MOSPD1 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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