TJP1 Gene TJP1 Deficiency Genetic Test
Test Name: TJP1 Gene TJP1 Deficiency Genetic Test
Components: TJP1 gene analysis
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Method: NGS Technology
Test Type: Metabolic Disorders
Doctor: General Physician
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for TJP1 Gene TJP1 deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TJP1 deficiency.
What is the TJP1 Gene?
TJP1, also known as tight junction protein 1, is a gene that encodes a protein involved in the formation and maintenance of tight junctions. Tight junctions are specialized structures that seal the space between cells in epithelial and endothelial tissues, playing a crucial role in maintaining tissue integrity and regulating the movement of molecules across cell layers.
Understanding TJP1 Deficiency
A deficiency in the TJP1 gene can lead to dysfunction in tight junctions, resulting in increased permeability of the epithelial or endothelial barrier. This can have various consequences depending on the affected tissues, including impaired absorption of nutrients, increased susceptibility to infections, and tissue damage.
NGS Genetic Testing for TJP1 Deficiency
NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, providing a comprehensive evaluation of an individual’s genetic makeup. In the context of TJP1 deficiency, NGS genetic testing can be used to identify mutations or variations in the TJP1 gene that may be associated with the condition.
By identifying specific genetic variants in TJP1, NGS genetic testing can help in diagnosing TJP1 deficiency and determining the underlying cause of the condition. This information can be crucial for appropriate management and treatment strategies for affected individuals. Additionally, NGS genetic testing can also help in identifying carriers of TJP1 mutations, allowing for genetic counseling and family planning.
| Test Name | TJP1 Gene TJP1 deficiency Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for TJP1 Gene TJP1 deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TJP1 deficiency |
| Test Details |
TJP1, also known as tight junction protein 1, is a gene that encodes a protein involved in the formation and maintenance of tight junctions. Tight junctions are specialized structures that seal the space between cells in epithelial and endothelial tissues, playing a crucial role in maintaining tissue integrity and regulating the movement of molecules across cell layers. A deficiency in the TJP1 gene can lead to dysfunction in tight junctions, resulting in increased permeability of the epithelial or endothelial barrier. This can have various consequences depending on the affected tissues, including impaired absorption of nutrients, increased susceptibility to infections, and tissue damage. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, providing a comprehensive evaluation of an individual’s genetic makeup. In the context of TJP1 deficiency, NGS genetic testing can be used to identify mutations or variations in the TJP1 gene that may be associated with the condition. By identifying specific genetic variants in TJP1, NGS genetic testing can help in diagnosing TJP1 deficiency and determining the underlying cause of the condition. This information can be crucial for appropriate management and treatment strategies for affected individuals. Additionally, NGS genetic testing can also help in identifying carriers of TJP1 mutations, allowing for genetic counseling and family planning. |
