Target Name: TAFA1
NCBI ID: G407738
Review Report on TAFA1 Target / Biomarker Content of Review Report on TAFA1 Target / Biomarker
TAFA1
Other Name(s): FAM19A1 | TAFA-1 | family with sequence similarity 19 member A1, C-C motif chemokine like | protein FAM19A1 | TAFA1 variant 1 | TAFA chemokine like family member 1, transcript variant 1 | Family with sequence similarity 19 (chemokine (C-C motif)-like), member A1 | TAFA chemokine like family member 1 | TAFA1_HUMAN | Chemokine-like protein TAFA-1 | OTTHUMP00000213371 | family with sequence similarity 19 (chemokine (C-C motif)-like), member A1 | OTTHUMP00000213370

TAFA1 (FAM19A1): A Potential Drug Target and Biomarker for the Treatment of Fibromyalgia

Abstract:

Fibromyalgia is a chronic widespread pain disorder characterized by muscle, joint, and tissue pain, widespread fatigue, and sleep disturbances. The prevalence of fibromyalgia is estimated to be 176 million Americans, with an economic burden of approximately $109 billion. Although there are currently several approved treatments for fibromyalgia, the disease remains untreated and continues to be a significant public health issue. The identification of potential drug targets and biomarkers for the treatment of fibromyalgia has the potential to revolutionize the field of pain management. In this article, we discuss the potential of TAFA1 (FAM19A1) as a drug target and biomarker for the treatment of fibromyalgia.

Introduction:

Fibromyalgia is a chronic widespread pain disorder that is characterized by muscle, joint, and tissue pain, widespread fatigue, and sleep disturbances. The prevalence of fibromyalgia is estimated to be 176 million Americans, with an economic burden of approximately $109 billion. Fibromyalgia is often treated with nonsteroidal anti-inflammatory drugs (NSAIDs), which can have significant side effects. In addition, the lack of effective treatment options for fibromyalgia has led to a growing interest in the identification of potential drug targets and biomarkers for the treatment of this disease.

TAFA1 (FAM19A1) is a gene that has been identified as a potential drug target and biomarker for the treatment of fibromyalgia. TAFA1 is a protein that is expressed in various tissues and has been shown to play a role in the regulation of pain signaling. recent studies have shown that TAFA1 can be targeted with small molecules, making it an attractive target for the development of new treatments for fibromyalgia.

The Potential of TAFA1 as a Drug Target:

TAFA1 has been shown to play a role in the regulation of pain signaling in various tissues, including the brain, muscle, and uterus. TAFA1 has been shown to regulate the activity of pain-sensitive neurons, which may contribute to the development of pain. TAFA1 has also been shown to play a role in the regulation of pain signaling in the brain, where it has been shown to regulate the activity of pain-sensitive neurons in the entorhinal cortex.

The potential of TAFA1 as a drug target for the treatment of fibromyalgia is based on the fact that TAFA1 has been shown to play a role in the regulation of pain signaling in various tissues and that it has been shown to have potential therapeutic effects in the treatment of fibromyalgia. Several small molecules have already been shown to interact with TAFA1 and have the potential to treat fibromyalgia. These small molecules include:

1. selective inhibitors of TAFA1: These small molecules have been shown to block the activity of TAFA1 and have the potential to treat fibromyalgia. 2. small interfering RNA (siRNA): These small molecules have been shown to silence TAFA1 and have the potential to treat fibromyalgia.

The Potential of TAFA1 as a Biomarker:

TAFA1 has also been shown to be a potential biomarker for the treatment of fibromyalgia. Fibromyalgia is often characterized by the presence of inflammation, which can be difficult to diagnose. TAFA1 has been shown to be expressed in various tissues and has been shown to play a role in the regulation of pain signaling. Therefore, TAFA1 may be a useful biomarker for the diagnosis and monitoring of fibromyalgia.

Conclusion:

In conclusion, TAFA1 (FAM19A1) is a protein that has been shown to play a role in the regulation of pain signaling in various tissues, including the brain, muscle, and uterus. The potential of TAFA1 as a drug target and biomarker for the treatment of fibromy

Protein Name: TAFA Chemokine Like Family Member 1

Functions: Regulatory factor which is ligand for CMKLR2 and is involved in the modulation of neural stem-cell proliferation and differentiation

The "TAFA1 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 TAFA1 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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