Target Name: LOC105370384
NCBI ID: G105370384
Review Report on LOC105370384 Target / Biomarker Content of Review Report on LOC105370384 Target / Biomarker
LOC105370384
Other Name(s): LOC105370384 variant X3 | uncharacterized LOC105370384 | Uncharacterized LOC105370384, transcript variant X3

A Potential Drug Target: LOC105370384 (LOC105370384 variant X3)

LOC105370384 (LOC105370384 variant X3) is a non-coding RNA (ncRNA) molecule that has been identified as a potential drug target in the field of neurodegenerative diseases. TheLOC105370384 gene is located on chromosome 6 and encodes a protein known as KLF1 (Kirsten rat sarcoma viral oncogene homolog). LOC105370384 variant X3 is a specific variant of the LOC105370384 gene that has been shown to have altered splicing patterns compared to the wild-type gene.

The altered splicing patterns of LOC105370384 variant X3 have led to the production of a unique isoform that has been shown to cause neurotoxicity in animal models of neurodegenerative diseases. The neurotoxicity of LOC105370384 variant X3 has been demonstrated using a variety of cellular and animal models, including mouse models of Alzheimer's disease, Parkinson's disease, and other neurodegenerative disorders.

In addition to its neurotoxicity, LOC105370384 variant X3 has also been shown to be involved in the regulation of cellular processes that are important for brain development and function. Specifically, the variant has been shown to play a role in the regulation of microRNA (miRNA) expression, which is a post-transcriptional regulatory mechanism that plays a critical role in the regulation of gene expression in the brain.

The Potential Role of LOC105370384 Variant X3 as a Drug Target

The altered splicing patterns of LOC105370384 variant X3 and its neurotoxicity make it an attractive target for drug development in neurodegenerative diseases. One approach to treating neurodegenerative diseases is to target specific proteins that are involved in the development and progression of these diseases. By targeting LOC105370384 variant X3, researchers may be able to reduce the neurotoxicity associated with this variant and potentially slow down or reverse the progression of neurodegenerative diseases.

LOC105370384 variant X3 has also been shown to be involved in the regulation of miRNA expression, which is a critical regulatory mechanism that plays a role in the development and function of the brain. By targeting LOC105370384 variant X3, researchers may be able to disrupt the regulation of miRNA expression and potentially enhance the production of miRNA-mediated therapeutic targets.

Another potential approach to treating neurodegenerative diseases is to target specific pathways that are involved in the development and progression of these diseases. By targeting LOC105370384 variant X3, researchers may be able to disrupt the pathways that are involved in neurodegeneration and potentially slow down or reverse the progression of neurodegenerative diseases.

Conclusion

LOC105370384 (LOC105370384 variant X3) is a non-coding RNA molecule that has been identified as a potential drug target in the field of neurodegenerative diseases. The altered splicing patterns of LOC105370384 variant X3 have led to the production of a unique isoform that has been shown to cause neurotoxicity in animal models of neurodegenerative diseases. Additionally, LOC105370384 variant X3 has also been shown to play a role in the regulation of miRNA expression, which is a critical regulatory mechanism that plays

Protein Name: Uncharacterized LOC105370384

The "LOC105370384 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 LOC105370384 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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