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SLCO1B1 Gene Hyperbilirubinemia Rotor Type Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The SLCO1B1 gene hyperbilirubinemia Rotor type genetic test is a sophisticated diagnostic tool designed to detect mutations in the SLCO1B1 gene, which are associated with Rotor syndrome. Rotor syndrome is a rare hereditary condition characterized by chronic, mild, predominantly conjugated hyperbilirubinemia without evidence of hemolysis or overt liver disease. Unlike other forms of genetic hyperbilirubinemia, Rotor syndrome does not lead to significant liver damage but can result in jaundice and bilirubinuria.

The test involves analyzing the patient’s DNA to identify specific genetic variations in the SLCO1B1 gene that are linked to the condition. This gene plays a crucial role in the hepatic uptake and processing of bilirubin, and mutations can disrupt these processes, leading to the accumulation of bilirubin in the blood.

Offered by DNA Labs UAE, this genetic test is priced at 4400 AED. The test is conducted in a state-of-the-art laboratory equipped with the latest genetic sequencing technology, ensuring high accuracy and reliability of results. It is a valuable diagnostic tool for individuals experiencing symptoms of hyperbilirubinemia or those with a family history of Rotor syndrome, enabling timely and appropriate management of the condition.

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SLCO1B1 Gene Hyperbilirubinemia Rotor type Genetic Test

At DNA Labs UAE, we offer the SLCO1B1 Gene Hyperbilirubinemia Rotor type Genetic Test at a cost of AED 4400.0.

Test Details

The SLCO1B1 gene is responsible for encoding a protein called organic anion transporting polypeptide 1B1 (OATP1B1). This protein is found in the liver and is involved in the transport of bilirubin, a yellow pigment produced during the breakdown of red blood cells.

Mutations in the SLCO1B1 gene can lead to a condition known as hyperbilirubinemia, Rotor type. Hyperbilirubinemia refers to high levels of bilirubin in the blood, which can cause yellowing of the skin and eyes (jaundice).

Rotor type hyperbilirubinemia is a relatively rare inherited disorder characterized by mild jaundice and elevated levels of bilirubin in the blood, but without any other liver abnormalities.

Test Components

  • Price: AED 4400.0
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Hepatology Nephrology Endocrinology Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the SLCO1B1 Gene Hyperbilirubinemia Rotor type Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with SLCO1B1 Gene Hyperbilirubinemia, Rotor type NGS Genetic DNA Test gene SLCO1B1.

NGS Technology

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the context of hyperbilirubinemia, NGS genetic testing can be used to identify mutations in the SLCO1B1 gene that may be causing the condition.

This type of testing can provide a comprehensive analysis of multiple genes, allowing for a more accurate diagnosis and potentially guiding treatment decisions.

It’s important to note that genetic testing should always be done under the guidance of a healthcare professional, such as a genetic counselor or medical geneticist, who can interpret the results and provide appropriate counseling and management recommendations.

Test Name SLCO1B1 Gene Hyperbilirubinemia Rotor type 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SLCO1B1 Gene Hyperbilirubinemia, Rotor type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLCO1B1 Gene Hyperbilirubinemia, Rotor type NGS Genetic DNA Test gene SLCO1B1
Test Details

The SLCO1B1 gene is responsible for encoding a protein called organic anion transporting polypeptide 1B1 (OATP1B1). This protein is found in the liver and is involved in the transport of bilirubin, a yellow pigment produced during the breakdown of red blood cells.

Mutations in the SLCO1B1 gene can lead to a condition known as hyperbilirubinemia, Rotor type. Hyperbilirubinemia refers to high levels of bilirubin in the blood, which can cause yellowing of the skin and eyes (jaundice). Rotor type hyperbilirubinemia is a relatively rare inherited disorder characterized by mild jaundice and elevated levels of bilirubin in the blood, but without any other liver abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the context of hyperbilirubinemia, NGS genetic testing can be used to identify mutations in the SLCO1B1 gene that may be causing the condition. This type of testing can provide a comprehensive analysis of multiple genes, allowing for a more accurate diagnosis and potentially guiding treatment decisions.

It’s important to note that genetic testing should always be done under the guidance of a healthcare professional, such as a genetic counselor or medical geneticist, who can interpret the results and provide appropriate counseling and management recommendations.

SKU: TEST-3652 Category:

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