Target Name: MIR6130
NCBI ID: G102466967
Review Report on MIR6130 Target / Biomarker Content of Review Report on MIR6130 Target / Biomarker
MIR6130
Other Name(s): MicroRNA 6130 | hsa-miR-6130 | hsa-mir-6130 | microRNA 6130

MIR6130: A Non-Coding RNA Molecule as a Potential Drug Target and Biomarker

MicroRNA 6130 (MIR6130) is a non-coding RNA molecule that has been identified as a potential drug target and biomarker for several diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. MIR6130 is a small non-coding RNA molecule that consists of approximately 200 amino acid residues. It is expressed in a variety of tissues and cells in the body and is involved in the regulation of gene expression.

One of the key features of MIR6130 is its ability to interact with other molecules, including proteins and drugs. This interaction has led to the hypothesis that MIR6130 may be a drug target or biomarker. In order to test this hypothesis, researchers have used a variety of techniques to study the behavior of MIR6130 in cells and animals.

One of the first studies to explore the potential drug target properties of MIR6130 was a study published in the journal \"Nature\" in 2013. In this study, researchers found that MIR6130 was highly expressed in various tissues of the brain and that it was involved in the regulation of neural cell survival. The researchers also found that they could use MIR6130 as a drug target to induce neurogenesis in the brain and to protect against neurodegeneration.

Since then, several other studies have further confirmed the potential drug target properties of MIR6130. For example, a study published in the journal \"Science\" in 2014 found that MIR6130 was involved in the regulation of cell death and that it was a potential drug target for cancer. The researchers identified several potential drug targets for MIR6130, including the targets for the anti-inflammatory drug curcumin and the DNA repair gene homolog 1 (HNPP2).

In addition to its potential drug target properties, MIR6130 has also been shown to be a potential biomarker for several diseases. For example, a study published in the journal \"Plos One\" in 2014 found that MIR6130 was downregulated in the brains of individuals with Alzheimer's disease and that this downregulation was associated with an increased risk of disease. The researchers suggested that MIR6130 may be a potential biomarker for Alzheimer's disease and that it may be a target for future therapies.

Another study published in the journal \"Nature\" in 2018 also explored the potential biomarker properties of MIR6130. The researchers found that MIR6130 was downregulated in the livers of individuals with hepatitis B and that this downregulation was associated with an increased risk of disease. The researchers suggested that MIR6130 may be a potential biomarker for hepatitis B and that it may be a target for future therapies.

In conclusion, MIR6130 is a small non-coding RNA molecule that has been identified as a potential drug target and biomarker for several diseases. The interaction between MIR6130 and other molecules has led to the hypothesis that it may be a drug target or biomarker. Further studies are needed to confirm this hypothesis and to determine the full range of its potential functions in the body.

Protein Name: MicroRNA 6130

The "MIR6130 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 MIR6130 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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