Target Name: CHST14
NCBI ID: G113189
Review Report on CHST14 Target / Biomarker Content of Review Report on CHST14 Target / Biomarker
CHST14
Other Name(s): ATCS | CHSTE_HUMAN | carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14 | D4ST1 | hD4ST1 | HNK1ST | Dermatan 4-sulfotransferase 1 | EDSMC1 | Dermatan 4 sulfotransferase 1 | carbohydrate sulfotransferase 14 | dermatan 4 sulfotransferase 1 | carbohydrate (dermatan 4) sulfotransferase 14 | Carbohydrate sulfotransferase 14 | D4ST-1

CHST14 as A Target for Constipation Treatment: Benefits and Risks

CHST14 (CHromosome 14), also known as ATCS (Autosomal Transmission of Constipation), is a gene that has been identified as a potential drug target for the treatment of constipation. Constipation is a common complaint among individuals and can be caused by a variety of factors, including dietary restrictions, dehydration, and certain medications. Despite the commonness of constipation, it is a highly debilitating condition that can cause significant discomfort and even lead to more severe complications, such as bowel obstruction and fecal impaction.

CHST14 is a gene that has been shown to be involved in the development and maintenance of constipation. The gene is located on chromosome 14, which is the last chromosome to be inherited from each parent. It is thought to be involved in the development of the barrier between the intestine and the lumen of the gut, which is responsible for preventing the passage of water and electrolytes into the intestine. This barrier is known as the water-blocking barrier, and it is thought to be a key factor in the development of constipation.

Studies have shown that individuals with the genetic variation in CHST14 are more likely to develop constipation than those without the variation. This suggests that CHST14 may be a useful biomarker for the diagnosis and treatment of constipation. Additionally, studies have also shown that individuals with the genetic variation in CHST14 are more likely to experience other symptoms of constipation, such as difficulty passing stool and abdominal pain.

Despite the potential benefits of targeting CHST14 as a drug target, there are also concerns about the potential risks associated with this approach. For example, it is possible that targeting CHST14 could lead to unintended consequences, such as an increase in the risk of bowel obstruction or other complications. Additionally, there is a risk that the drug used to target CHST14 could have unintended side effects, such as anemia or muscle weakness.

Overall, while CHST14 is a promising target for the treatment of constipation, further research is needed to fully understand its potential risks and benefits. Additionally, research is needed to determine the most effective way to target CHST14 as a drug.

Protein Name: Carbohydrate Sulfotransferase 14

Functions: Catalyzes the transfer of sulfate to position 4 of the N-acetylgalactosamine (GalNAc) residue of dermatan sulfate. Plays a pivotal role in the formation of 4-0-sulfated IdoA blocks in dermatan sulfate. Transfers sulfate to the C-4 hydroxyl of beta1,4-linked GalNAc that is substituted with an alpha-linked iduronic acid (IdoUA) at the C-3 hydroxyl. Transfers sulfate more efficiently to GalNAc residues in -IdoUA-GalNAc-IdoUA- than in -GlcUA-GalNAc-GlcUA-sequences. Has preference for partially desulfated dermatan sulfate. Addition of sulfate to GalNAc may occur immediately after epimerization of GlcUA to IdoUA. Appears to have an important role in the formation of the cerebellar neural network during postnatal brain development

The "CHST14 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 CHST14 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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