Trait
Increased CSF interferon alpha
Increased concentration of interferon alpha in the cerebrospinal fluid (CSF).
Summary
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/increased-csf-interferon-alpha.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Increased CSF interferon alpha, and the rest of your genome, with one test.
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Get my Genome Test9 genes linked to Increased CSF interferon alpha
Changes in these genes cause rare conditions in which Increased CSF interferon alpha is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ADARadenosine deaminase RNA specific | Always | In 2 conditions |
| TREX1three prime repair exonuclease 1 | Always | In 2 conditions |
| IFIH1interferon induced with helicase C domain 1 | Often (30–79%) | In 1 condition |
| LSM11LSM11, U7 small nuclear RNA associated | Often (30–79%) | In 1 condition |
| RNASEH2Aribonuclease H2 subunit A | Often (30–79%) | In 1 condition |
| RNASEH2Bribonuclease H2 subunit B | Often (30–79%) | In 1 condition |
| RNASEH2Cribonuclease H2 subunit C | Often (30–79%) | In 1 condition |
| RNU7-1RNA, U7 small nuclear 1 | Often (30–79%) | In 1 condition |
| SAMHD1SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 | Often (30–79%) | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.17-8666dff2.
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