Target Name: RPL17
NCBI ID: G6139
Review Report on RPL17 Target / Biomarker Content of Review Report on RPL17 Target / Biomarker
RPL17
Other Name(s): gene encoding putative NFkB activating protein | PD-1 | RPL17-C18orf32 readthrough | RPL17-C18orf32 protein | RL17_HUMAN | large ribosomal subunit protein uL22 | L17 | RPL23 | Ribosomal protein L17 | Large ribosomal subunit protein uL22 | ribosomal protein L17 | 60S ribosomal protein L17 | RPL17 variant 1 | 60S ribosomal protein L17 (isoform a) | Ribosomal protein L17, transcript variant 1 | 60S ribosomal protein L23

RPL17: A Potential Drug Target for FTD

The protein encoded by the gene RPL17 is a potential drug target or biomarker associated with the neurodegenerative disorder frontotemporal dementia (FTD). Frontotemporal dementia is a progressive neurodegenerative disorder that affects the frontal and temporal regions of the brain, leading to a range of symptoms including memory loss, decline in cognitive function, and personality changes. The exact cause of FTD is not known, but research has identified genetic and neurochemical changes that are thought to contribute to its development.

The RPL17 gene

The RPL17 gene is located on chromosome 16 and encodes a protein known as putative NFkB activating protein (NFAP). NFAP is a key regulator of nuclear factor kappa B (NFkB), a protein that plays a role in cell signaling and inflammation. Mutations in the RPL17 gene have been linked to a variety of neurological and psychiatric disorders, including FTD.

The role of NFAP in FTD

The exact function of NFAP in FTD is not well understood, but research has suggested that it may be involved in the regulation of cellular processes that are important for the development and progression of the disease. One potential role for NFAP in FTD is in the regulation of inflammation.

Studies have shown that individuals with FTD are often characterized by increased inflammation in their brains, which is thought to contribute to the development and progression of the disease. NFAP has been shown to play a role in the regulation of inflammatory responses, and may be involved in the regulation of the immune system's response to infection.

Another potential role for NFAP in FTD is in the regulation of cellular signaling pathways that are important for the development and progression of the disease. For example, studies have shown that individuals with FTD have altered levels of neurotransmitters, such as dopamine, in their brains, which may be related to the regulation of signaling pathways that are important for the transmission of neural information.

The potential therapeutic benefits of targeting RPL17

Targeting RPL17 as a drug target or biomarker may have therapeutic benefits for the treatment of FTD. By inhibiting the activity of NFAP, researchers may be able to reduce the inflammation and cellular signaling pathways that are thought to contribute to the development and progression of the disease. This could potentially lead to the development of new treatments for FTD, including medications that can slow the progression of the disease or even reverse its effects.

Current research on RPL17

While more research is needed to fully understand the role of RPL17 in FTD, studies have shown that targeting the gene has the potential to be a promising therapeutic approach. One potential approach to targeting RPL17 is to develop small molecules that can inhibit the activity of NFAP. This approach has been used to develop new treatments for a variety of neurological and psychiatric disorders, including Alzheimer's disease and depression.

Another potential approach to targeting RPL17 is to use RNA interference (RNAi) technology to knock down the levels of RPL17 in the brains of individuals with FTD. RNAi has been shown to be effective in reducing the levels of proteins in the brains of individuals with a variety of neurological and psychiatric disorders, and may be a useful approach to targeting RPL17 in FTD.

Conclusion

In conclusion, the protein encoded by the gene RPL17 is a potential drug target or biomarker associated with the neurodegenerative disorder frontotemporal dementia (FTD). Research has suggested that RPL17 may be involved in the regulation of cellular processes that are important for the development and progression of the disease, including inflammation and cellular signaling pathways. Targeting RPL17 as a drug target or biomarker may have therapeutic benefits for the treatment of FTD, including the development of new treatments for the disease. Further research is needed to fully understand the role of RPL17 in FTD and to develop effective treatments for this debilitating and often progressive

Protein Name: Ribosomal Protein L17

Functions: Component of the large ribosomal subunit (PubMed:12962325, PubMed:23636399, PubMed:32669547). The ribosome is a large ribonucleoprotein complex responsible for the synthesis of proteins in the cell (PubMed:12962325, PubMed:23636399, PubMed:32669547)

The "RPL17 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 RPL17 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

More Common Targets

RPL17P25 | RPL17P33 | RPL17P34 | RPL17P39 | RPL17P4 | RPL17P44 | RPL17P49 | RPL17P7 | RPL17P8 | RPL18 | RPL18A | RPL18AP16 | RPL18AP3 | RPL18AP6 | RPL18AP8 | RPL18P1 | RPL18P13 | RPL18P4 | RPL19 | RPL19P12 | RPL19P21 | RPL19P4 | RPL19P8 | RPL21 | RPL21P108 | RPL21P119 | RPL21P131 | RPL21P133 | RPL21P134 | RPL21P14 | RPL21P16 | RPL21P19 | RPL21P2 | RPL21P20 | RPL21P28 | RPL21P33 | RPL21P39 | RPL21P42 | RPL21P44 | RPL21P53 | RPL21P7 | RPL21P97 | RPL21P98 | RPL22 | RPL22L1 | RPL22P1 | RPL23 | RPL23A | RPL23AP1 | RPL23AP12 | RPL23AP16 | RPL23AP2 | RPL23AP21 | RPL23AP25 | RPL23AP3 | RPL23AP32 | RPL23AP34 | RPL23AP42 | RPL23AP43 | RPL23AP44 | RPL23AP45 | RPL23AP5 | RPL23AP53 | RPL23AP56 | RPL23AP57 | RPL23AP6 | RPL23AP61 | RPL23AP63 | RPL23AP64 | RPL23AP7 | RPL23AP79 | RPL23AP82 | RPL23AP87 | RPL23P6 | RPL23P8 | RPL24 | RPL24P2 | RPL24P7 | RPL26 | RPL26L1 | RPL26L1-AS1 | RPL26P12 | RPL26P13 | RPL26P21 | RPL26P30 | RPL26P32 | RPL26P36 | RPL27 | RPL27A | RPL27AP6 | RPL27P11 | RPL28 | RPL28P1 | RPL29 | RPL29P11 | RPL29P12 | RPL29P14 | RPL29P19 | RPL29P2 | RPL29P20