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Trait
Corneal inflammation
Clinical name: Keratitis
Inflammation of the cornea.
Summary
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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/keratitis.json"
page <- fromJSON(url)
page$trait$nameCorneal inflammationHP:0000491
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Get my Genome Test51 genes linked to Corneal inflammation
Changes in these genes cause rare conditions in which Corneal inflammation 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 |
|---|---|---|
| GJB2gap junction protein beta 2 | Always | In 2 conditions |
| IL6STinterleukin 6 cytokine family signal transducer | Always | In 1 condition |
| NLRP3NLR family pyrin domain containing 3 | Always | In 1 condition |
| PAX6paired box 6 | Always | In 2 conditions |
| NOD2nucleotide binding oligomerization domain containing 2 | Very often (80–99%) | In 1 condition |
| ABCA12ATP binding cassette subfamily A member 12 | Often (30–79%) | In 2 conditions |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Often (30–79%) | In 2 conditions |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Often (30–79%) | In 2 conditions |
| CERS3ceramide synthase 3 | Often (30–79%) | In 1 condition |
| CLTCL1clathrin heavy chain like 1 | Often (30–79%) | In 1 condition |
| DDB2damage specific DNA binding protein 2 | Often (30–79%) | In 2 conditions |
| DNMT3BDNA methyltransferase 3 beta | Often (30–79%) | In 1 condition |
| DUX4double homeobox 4 | Often (30–79%) | In 1 condition |
| DUX4L1double homeobox 4 like 1 (pseudogene) | Often (30–79%) | In 1 condition |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Often (30–79%) | In 2 conditions |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Often (30–79%) | In 1 condition |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Often (30–79%) | In 1 condition |
| ERCC5ERCC excision repair 5, endonuclease | Often (30–79%) | In 1 condition |
| FRG1FSHD region gene 1 | Often (30–79%) | In 1 condition |
| GJB6gap junction protein beta 6 | Often (30–79%) | In 1 condition |
| NIPAL4NIPA like domain containing 4 | Often (30–79%) | In 2 conditions |
| PNPLA1patatin like domain 1, omega-hydroxyceramide transacylase | Often (30–79%) | In 1 condition |
| POLHDNA polymerase eta | Often (30–79%) | In 2 conditions |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Often (30–79%) | In 2 conditions |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Often (30–79%) | In 1 condition |
| SREBF1sterol regulatory element binding transcription factor 1 | Often (30–79%) | In 1 condition |
| SULT2B1sulfotransferase family 2B member 1 | Often (30–79%) | In 2 conditions |
| TGM1transglutaminase 1 | Often (30–79%) | In 2 conditions |
| TP63tumor protein p63 | Often (30–79%) | In 1 condition |
| XPAXPA, DNA damage recognition and repair factor | Often (30–79%) | In 2 conditions |
| XPCXPC complex subunit, DNA damage recognition and repair factor | Often (30–79%) | In 2 conditions |
| ASPRV1aspartic peptidase retroviral like 1 | Sometimes (5–29%) | In 1 condition |
| COL4A5collagen type IV alpha 5 chain | Sometimes (5–29%) | In 1 condition |
| COL4A6collagen type IV alpha 6 chain | Sometimes (5–29%) | In 1 condition |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Sometimes (5–29%) | In 1 condition |
| CYP4F22cytochrome P450 family 4 subfamily F member 22 | Sometimes (5–29%) | In 1 condition |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Sometimes (5–29%) | In 1 condition |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Sometimes (5–29%) | In 1 condition |
| LIPNlipase family member N | Sometimes (5–29%) | In 1 condition |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Sometimes (5–29%) | In 3 conditions |
Show 11 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| PRTN3proteinase 3 | Sometimes (5–29%) | In 1 condition |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Sometimes (5–29%) | In 1 condition |
| SLC35C1solute carrier family 35 member C1 | Sometimes (5–29%) | In 1 condition |
| WASWASP actin nucleation promoting factor | Sometimes (5–29%) | In 1 condition |
| CRLF1cytokine receptor like factor 1 | Not recorded | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Not recorded | In 1 condition |
| FGFR2fibroblast growth factor receptor 2 | Not recorded | In 1 condition |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Not recorded | In 1 condition |
| NTRK1neurotrophic receptor tyrosine kinase 1 | Not recorded | In 1 condition |
| PLECplectin | Not recorded | In 1 condition |
| ZEB1zinc finger E-box binding homeobox 1 | Not recorded | 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.
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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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