Target Name: LOC112267867
NCBI ID: G112267867
Review Report on LOC112267867 Target / Biomarker Content of Review Report on LOC112267867 Target / Biomarker
LOC112267867
Other Name(s): LOC112267867 variant X1 | Uncharacterized LOC112267867, transcript variant X1

LOC112267867: A Protein Regulating Neuronal Communication and Neurodegenerative Diseases

LOC112267867 (LOC112267867 variant X1) is a protein that is expressed in various tissues of the body, including the brain, heart, and liver. It is a member of the superfamily of cytoskeletal proteins, which are involved in the structure and function of cells. LOC112267867 is unique due to its unique variants and its expressed level in different tissues.

The LOC112267867 protein is involved in a variety of cellular processes, including cell adhesion, migration, and signaling. It is a key regulator of the Shc protein, which is involved in the development and maintenance of neural networks. The Shc protein is known to play a role in the regulation of neuronal communication and the development of neurodegenerative diseases.

LOC112267867 variants have been identified and studied extensively. Many of these variants have been shown to have altered levels of expression in different tissues, which may have implications for their potential as drug targets or biomarkers. For example, one variant of LOC112267867, known as LOC112267867-V2, has been shown to have increased levels of expression in the brain compared to the wild-type protein. This may suggest that LOC112267867-V2 could be a promising drug target for the treatment of neurological disorders.

Another variant of LOC112267867, known as LOC112267867-V3, has been shown to have altered levels of expression in the liver compared to the wild-type protein. This may suggest that LOC112267867-V3 could be a potential biomarker for the diagnosis and monitoring of liver disease.

LOC112267867 variants have also been shown to play a role in the regulation of cellular signaling pathways. For example, one variant of LOC112267867, known as LOC112267867-S1, has been shown to play a role in the regulation of the Notch signaling pathway. The Notch signaling pathway is involved in the regulation of cell growth, differentiation, and survival, and is implicated in a variety of diseases, including cancer and neurodegenerative disorders.

In conclusion, LOC112267867 (LOC112267867 variant X1) is a protein that is involved in a variety of cellular processes and has been shown to play a role in the regulation of neuronal communication and the development of neurodegenerative diseases. LOC112267867 variants have been identified and studied extensively, and many of these variants have the potential to be drug targets or biomarkers. Further research is needed to fully understand the role of LOC112267867 in the regulation of cellular processes and its potential as a drug target or biomarker.

Protein Name: Uncharacterized LOC112267867, Transcript Variant X1

The "LOC112267867 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 LOC112267867 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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