Genetic sequencing analysis of the MRPS22 gene (full mutation detection)
This test checks for specific genetic changes (mutations) in the MRPS22 gene, which may be linked to certain inherited conditions affecting muscle or other body functions.
["This test helps identify if you carry mutations in the MRPS22 gene that could influence your health."]
Key facts at a glance
- LOINC
- 77096-6
- Short code
- MRPS22 Full Mut Anl Bld/T Seq
- Synonyms
- MRPS22 Full Mut Anl Bld/T Seq
- Category
- chemistry
- Sample
- whole-blood
- Container
- Lavender-top (EDTA)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- sequencing
- Specimen volume
- 3 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h
- Hemolysis max
- 0
- Lipemia max
- 0
- Icterus max
- 0
- TAT
- 4–24 hours
- Order
- routine
What This Test Measures
The MRPS22 gene provides instructions for making a protein that is essential for proper cell function, particularly in muscle tissue. Mutations in this gene can lead to rare genetic disorders. This test analyzes the DNA sequence of the MRPS22 gene to detect any full mutations present in your blood sample.
Why It Might Be Ordered
Your healthcare provider may recommend this test if you have symptoms of a genetic disorder linked to MRPS22 mutations, such as muscle weakness, developmental delays, or other related health concerns. It may also be used in genetic counseling or for carrier testing in families with a history of such conditions.
Sample Collection and Process
A blood sample is collected from you, typically through a simple venipuncture. The blood is then processed to extract DNA for genetic sequencing. This test does not measure a traditional lab analyte but instead examines the genetic code for specific mutations.
What to Expect Before the Test
No special preparation is needed for this test. You may eat and drink normally on the day of your appointment. If you are pregnant or have a history of bleeding disorders, inform your healthcare provider before the test.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
This test is used to diagnose or confirm suspected genetic disorders caused by MRPS22 mutations. It can also assist in genetic counseling, prenatal testing, or determining risk for passing these mutations to offspring. Results may help guide treatment options or management plans tailored to your condition.
Short name
MRPS22 Mutation Genetic Test
Frequently asked questions
How long will it take to get my results?
What do my results mean?
Can I have this test if I am pregnant?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy