LINC00518: A Gene Associated with A Variety of Diseases (G221718)

Target Name: LINC00518

NCBI ID: G221718

LINC00518

Other Name(s): C6orf218 | Long intergenic non-protein coding RNA 518 | long intergenic non-protein coding RNA 518

LINC00518: A Gene Associated with A Variety of Diseases

LINC00518 is a gene that encodes for a protein known as C6orf218. C6orf218 is a protein that is expressed in cells of nearly all human tissues, including neurons, liver, kidney, heart and muscle tissue. Its function has not yet been fully revealed, but research suggests that it may be involved in a variety of diseases.

Among them, variants of LINC00518 have been shown to be associated with a variety of neurological diseases. For example, variants of LINC00518 have been found in the brains of Parkinson's disease patients, who exhibit characteristics of neuronal death and loss of neuronal synapses. In addition, variants of LINC00518 have been found in the brains of Alzheimer's disease patients, who also show characteristics of neuronal death and loss of neuronal synapses.

In addition to its association with neurological diseases, variants of LINC00518 have also been found in other diseases, such as liver disease and kidney disease. These diseases are associated with neuronal death and loss of neuronal synapses, so variants of LINC00518 may also have biological significance in these diseases.

Variants of LINC00518 can also cause other types of cancer. For example, variants of LINC00518 have been found in multiple types of cancer, including breast, lung and kidney cancers. These cancers are associated with neuronal death and loss of neuronal synapses, so variants of LINC00518 may also have biological significance in these cancers.

In addition to its association with neurological disease, liver disease, kidney disease and cancer, variants of LINC00518 can cause other types of disease. For example, variants of LINC00518 have been found in autoimmune diseases that are associated with neuronal death and loss of neuronal synapses. In addition, variants of LINC00518 have been found in some genetic diseases, such as spinal muscular atrophy and congenital retinal agenesis.

To sum up, LINC00518 is a very important gene and is related to many diseases. Studying variants of LINC00518 could provide us with valuable information about diseases such as neurological disease, liver disease, kidney disease and cancer. Variants of LINC00518 may also become a new drug target or biomarker, providing new methods for treating these diseases.

Protein Name: Long Intergenic Non-protein Coding RNA 518

The "LINC00518 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 LINC00518 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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