What is U1-snRNP A and Why Does the Immune Zoomer Test for It?

Spliceosome U1 ribonucleoprotein antigen
U1-snRNP A is an RNA-binding protein that helps process pre-messenger RNA as part of the U1 small nuclear ribonucleoprotein complex. Measuring immune reactivity to this protein can reveal whether the immune system is targeting spliceosomal nuclear components and helps map broader patterns of immune activity.
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About U1-snRNP A
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U1-snRNP A FAQs

What is U1-snRNP A and why is it important?
U1‑snRNP A is a protein in the nucleus that helps cells edit messenger RNA before it makes proteins. The immune system can sometimes produce antibodies that bind to this protein. Detecting those antibodies helps show whether the immune system is reacting to core nuclear machinery, which can clarify complex symptom patterns when viewed alongside other markers.
What does it mean if my U1-snRNP A levels are low?
Low or undetectable U1‑snRNP A antibody levels mean the test did not find a measurable immune response to this specific nuclear protein. This can be a normal result or reflect timing, low antibody production, or testing limits. High levels, by contrast, indicate detectable immune reactivity to the target; both high and low results are best interpreted with other Immune Zoomer findings and clinical context.
What does it mean if my U1-snRNP A levels are high?
Elevated U1‑snRNP A antibody levels indicate measurable immune reactivity against a spliceosomal nuclear protein. Such reactivity can be part of broader systemic immune activity and may appear with other autoantibodies. Clinical interpretation requires the full panel and provider assessment to understand how this marker fits observed symptoms and other test results.
Why is this biomarker included in the Immune Zoomer?
Including U1‑snRNP A helps detect immune targeting of nuclear spliceosome components, adding depth to the Systemic Immune Activity domain. It improves pattern recognition across multiple autoantibodies, helping providers link immune signals to symptom clusters and prioritize further evaluation in a precision-testing framework.

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