Trait
Uveitis
Inflammation of one or all portions of the uveal tract.
Summary
Reference genomeGRCh38hg38
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Get my Genome Test42 genes linked to Uveitis
Changes in these genes cause rare conditions in which Uveitis 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 |
|---|---|---|
| GJA1gap junction protein alpha 1 | Always | In 1 condition |
| NLRP3NLR family pyrin domain containing 3 | Always | In 4 conditions |
| ANKRD55ankyrin repeat domain 55 | Often (30–79%) | In 2 conditions |
| BTNL2butyrophilin like 2 | Often (30–79%) | In 2 conditions |
| CD247CD247 molecule | Often (30–79%) | In 2 conditions |
| CD4CD4 molecule | Often (30–79%) | In 1 condition |
| DNASE1L3deoxyribonuclease 1L3 | Often (30–79%) | In 1 condition |
| FASFas cell surface death receptor | Often (30–79%) | In 2 conditions |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Often (30–79%) | In 3 conditions |
| IL2RAinterleukin 2 receptor subunit alpha | Often (30–79%) | In 2 conditions |
| IL2RBinterleukin 2 receptor subunit beta | Often (30–79%) | In 2 conditions |
| IRF4interferon regulatory factor 4 | Often (30–79%) | In 1 condition |
| NLRP1NLR family pyrin domain containing 1 | Often (30–79%) | In 1 condition |
| NOD2nucleotide binding oligomerization domain containing 2 | Often (30–79%) | In 1 condition |
| PTPN2protein tyrosine phosphatase non-receptor type 2 | Often (30–79%) | In 2 conditions |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Often (30–79%) | In 3 conditions |
| STAT4signal transducer and activator of transcription 4 | Often (30–79%) | In 2 conditions |
| TKTtransketolase | Often (30–79%) | In 2 conditions |
| AIREautoimmune regulator | Sometimes (5–29%) | In 1 condition |
| ATOH7atonal bHLH transcription factor 7 | Sometimes (5–29%) | In 1 condition |
| BLMBLM RecQ like helicase | Sometimes (5–29%) | In 1 condition |
| CD27CD27 molecule | Sometimes (5–29%) | In 1 condition |
| CHD6chromodomain helicase DNA binding protein 6 | Sometimes (5–29%) | In 1 condition |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Sometimes (5–29%) | In 1 condition |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Sometimes (5–29%) | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Sometimes (5–29%) | In 2 conditions |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Sometimes (5–29%) | In 2 conditions |
| HLA-Bmajor histocompatibility complex, class I, B | Sometimes (5–29%) | In 1 condition |
| LRBALPS responsive beige-like anchor protein | Sometimes (5–29%) | In 1 condition |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Sometimes (5–29%) | In 1 condition |
| TNFRSF1ATNF receptor superfamily member 1A | Sometimes (5–29%) | In 1 condition |
| XIAPX-linked inhibitor of apoptosis | Sometimes (5–29%) | In 1 condition |
| AP1S3adaptor related protein complex 1 subunit sigma 3 | Rarely (1–4%) | In 1 condition |
| CASP10caspase 10 | Rarely (1–4%) | In 1 condition |
| FASLGFas ligand | Rarely (1–4%) | In 1 condition |
| GPR35G protein-coupled receptor 35 | Rarely (1–4%) | In 1 condition |
| IL36RNinterleukin 36 receptor antagonist | Rarely (1–4%) | In 1 condition |
| MST1macrophage stimulating 1 | Rarely (1–4%) | In 1 condition |
| SEMA4Dsemaphorin 4D | Rarely (1–4%) | In 1 condition |
| TCF4transcription factor 4 | Rarely (1–4%) | In 1 condition |
Show 2 more genes
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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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 2026.10.16-c6eea6bf.
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