Target Name: SPNS3
NCBI ID: G201305
Review Report on SPNS3 Target / Biomarker Content of Review Report on SPNS3 Target / Biomarker
SPNS3
Other Name(s): SPNS sphingolipid transporter 3 (putative) | sphingolipid transporter 3 (putative) | Sphingolipid transporter 3 (putative), transcript variant 1 | solute carrier family 63 member 3 | Protein spinster homolog 3 | SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative) | SLC63A3 | SPNS3_HUMAN | SPNS3 variant 1 | SLC62A3 | Protein spinster homolog 3 (isoform 1) | spinster homolog 3

SPNS3: A Potential Drug Target and Biomarker forSPhingolipid Transporter 3

SPhingolipid Transporter 3 (SPNS3) is a protein that plays a crucial role in the transport of sphingomyelins, a type of lipid molecule, in the cell membrane. It is a member of the Spark family of transporters and is expressed in various tissues, including the brain, heart, and blood vessels. SPNS3 is essential for the proper functioning of these tissues and is involved in the regulation of various cellular processes, including inflammation, metabolism, and signaling pathways.

SPNS3 has been identified as a potential drug target due to its involvement in several diseases, including obesity, diabetes, and cardiovascular disease. It has been shown to play a role in the regulation of lipid metabolism and to contribute to the development of certain diseases.

One of the key functions of SPNS3 is its role in the transport of sphingomyelins. These lipid molecules are involved in various cellular processes, including cell signaling, energy storage, and inflammation. SPNS3 is thought to regulate the amount of sphingomyelins that are transported into the cell, which can have a significant impact on the levels of these molecules in the cell membrane.

SPNS3 is also involved in the regulation of inflammation. It has been shown to play a role in the production of pro-inflammatory cytokines, such as TNF-伪, IL-1尾, and IL-6. These cytokines can contribute to the development of various inflammatory diseases, including obesity, diabetes, and cardiovascular disease.

SPNS3 is also involved in the regulation of cellular signaling pathways. It has been shown to play a role in the regulation of several signaling pathways, including the TGF-β pathway, the Wnt pathway, and the G-protein-coupled receptor (GPCR) signaling pathway. These pathways can contribute to the development of various diseases, including obesity and cardiovascular disease.

In addition to its involvement in the regulation of sphingomyelins and cellular signaling pathways, SPNS3 is also thought to play a role in the regulation of cellular organization. It is a member of the Spark family of transporters, which are known for their ability to regulate the organization and dynamics of various cellular structures, including the cell membrane.

SPNS3 is also expressed in various tissues, including the brain, heart, and blood vessels. It is thought to play a role in the regulation of various cellular processes in these tissues, including the transport of lipid molecules and the production of pro-inflammatory cytokines.

Given its involvement in the regulation of sphingomyelins, inflammation, and cellular signaling pathways, it is possible that SPNS3 could be a drug target for the treatment of various diseases, including obesity, diabetes, and cardiovascular disease. Further research is needed to confirm this potential and to develop effective treatments for these diseases.

Protein Name: SPNS Lysolipid Transporter 3, Sphingosine-1-phosphate (putative)

Functions: Sphingolipid transporter

The "SPNS3 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 SPNS3 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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