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Trait
Mouth sore
Clinical name: Oral ulcer
Erosion of the mucous mebrane of the mouth with local excavation of the surface, resulting from the sloughing of inflammatory necrotic tissue.
Summary
- Also called
- Mouth ulcer, Oral mucosal ulceration
- Body system
- Abnormality of head or neck
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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/oral-ulcer.json"
page <- fromJSON(url)
page$trait$nameMouth soreHP:0000155
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Get my Genome Test76 genes linked to Mouth sore
Changes in these genes cause rare conditions in which Mouth sore 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 |
|---|---|---|
| ADA2adenosine deaminase 2 | Always | In 1 condition |
| C1QBcomplement C1q B chain | Always | In 1 condition |
| ELF4E74 like ETS transcription factor 4 | Always | In 1 condition |
| IL10RAinterleukin 10 receptor subunit alpha | Always | In 1 condition |
| LYNLYN proto-oncogene, Src family tyrosine kinase | Always | In 1 condition |
| RELARELA proto-oncogene, NF-kB subunit | Always | In 1 condition |
| STAT4signal transducer and activator of transcription 4 | Always | In 4 conditions |
| TNFAIP3TNF alpha induced protein 3 | Always | In 2 conditions |
| ZAP70zeta chain of T cell receptor associated protein kinase 70 | Always | In 1 condition |
| C4Acomplement C4A (Chido/Rodgers blood group) | Very often (80–99%) | In 2 conditions |
| CCR1C-C motif chemokine receptor 1 | Very often (80–99%) | In 1 condition |
| ERAP1endoplasmic reticulum aminopeptidase 1 | Very often (80–99%) | In 1 condition |
| FASFas cell surface death receptor | Very often (80–99%) | In 1 condition |
| HLA-Bmajor histocompatibility complex, class I, B | Very often (80–99%) | In 1 condition |
| IFNGR1interferon gamma receptor 1 | Very often (80–99%) | In 1 condition |
| IL10interleukin 10 | Very often (80–99%) | In 2 conditions |
| IL12Ainterleukin 12A | Very often (80–99%) | In 1 condition |
| IL12A-AS1IL12A antisense RNA 1 | Very often (80–99%) | In 1 condition |
| IL23Rinterleukin 23 receptor | Very often (80–99%) | In 1 condition |
| KLRC4killer cell lectin like receptor C4 | Very often (80–99%) | In 1 condition |
| MEFVMEFV innate immunity regulator, pyrin | Very often (80–99%) | In 1 condition |
| TLR4toll like receptor 4 | Very often (80–99%) | In 1 condition |
| UBAC2UBA domain containing 2 | Very often (80–99%) | In 1 condition |
| CATcatalase | Often (30–79%) | In 2 conditions |
| CD40LGCD40 ligand | Often (30–79%) | In 1 condition |
| CLPBClpB family mitochondrial disaggregase | Often (30–79%) | In 1 condition |
| DNASE1deoxyribonuclease 1 | Often (30–79%) | In 2 conditions |
| ELANEelastase, neutrophil expressed | Often (30–79%) | In 3 conditions |
| FCGR2AFc gamma receptor IIa | Often (30–79%) | In 1 condition |
| FCGR2BFc gamma receptor IIb | Often (30–79%) | In 2 conditions |
| GFI1growth factor independent 1 transcriptional repressor | Often (30–79%) | In 1 condition |
| MVKmevalonate kinase | Often (30–79%) | In 1 condition |
| RIPK1receptor interacting serine/threonine kinase 1 | Often (30–79%) | In 1 condition |
| SRP19signal recognition particle 19 | Often (30–79%) | In 1 condition |
| TAFAZZINtafazzin, phospholipid-lysophospholipid transacylase | Often (30–79%) | In 1 condition |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Often (30–79%) | In 1 condition |
| TLR7toll like receptor 7 | Often (30–79%) | In 2 conditions |
| TREX1three prime repair exonuclease 1 | Often (30–79%) | In 2 conditions |
| BANK1B cell scaffold protein with ankyrin repeats 1 | Sometimes (5–29%) | In 1 condition |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Sometimes (5–29%) | In 1 condition |
Show 36 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| C4Bcomplement C4B (Chido/Rodgers blood group) | Sometimes (5–29%) | In 1 condition |
| CD27CD27 molecule | Sometimes (5–29%) | In 1 condition |
| CR2complement C3d receptor 2 | Sometimes (5–29%) | In 1 condition |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Sometimes (5–29%) | In 1 condition |
| CYBC1cytochrome b-245 chaperone 1 | Sometimes (5–29%) | In 1 condition |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Sometimes (5–29%) | In 2 conditions |
| DOCK11dedicator of cytokinesis 11 | Sometimes (5–29%) | In 1 condition |
| ETS1ETS proto-oncogene 1, transcription factor | Sometimes (5–29%) | In 1 condition |
| FCGR3BFc gamma receptor IIIb | Sometimes (5–29%) | In 1 condition |
| G6PC3glucose-6-phosphatase catalytic subunit 3 | Sometimes (5–29%) | In 1 condition |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sometimes (5–29%) | In 1 condition |
| IGHG1immunoglobulin heavy constant gamma 1 (G1m marker) | Sometimes (5–29%) | In 1 condition |
| IL7Rinterleukin 7 receptor | Sometimes (5–29%) | In 2 conditions |
| IRAK1interleukin 1 receptor associated kinase 1 | Sometimes (5–29%) | In 2 conditions |
| IRF5interferon regulatory factor 5 | Sometimes (5–29%) | In 1 condition |
| ITGAMintegrin subunit alpha M | Sometimes (5–29%) | In 1 condition |
| JAZF1JAZF zinc finger 1 | Sometimes (5–29%) | In 1 condition |
| KIAA0319LKIAA0319 like | Sometimes (5–29%) | In 1 condition |
| MAP2K1mitogen-activated protein kinase kinase 1 | Sometimes (5–29%) | In 1 condition |
| MECP2methyl-CpG binding protein 2 | Sometimes (5–29%) | In 1 condition |
| NOD2nucleotide binding oligomerization domain containing 2 | Sometimes (5–29%) | In 1 condition |
| NRASNRAS proto-oncogene, GTPase | Sometimes (5–29%) | In 1 condition |
| PDCD1programmed cell death 1 | Sometimes (5–29%) | In 1 condition |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Sometimes (5–29%) | In 1 condition |
| PXKPX domain containing serine/threonine kinase like | Sometimes (5–29%) | In 1 condition |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| SLC37A4solute carrier family 37 member 4 | Sometimes (5–29%) | In 2 conditions |
| SPP1secreted phosphoprotein 1 | Sometimes (5–29%) | In 2 conditions |
| SYKspleen associated tyrosine kinase | Sometimes (5–29%) | In 1 condition |
| TNFSF4TNF superfamily member 4 | Sometimes (5–29%) | In 1 condition |
| TNIP1TNFAIP3 interacting protein 1 | Sometimes (5–29%) | In 1 condition |
| UBE2L3ubiquitin conjugating enzyme E2 L3 | Sometimes (5–29%) | In 1 condition |
| EFL1elongation factor like GTPase 1 | Rarely (1–4%) | In 1 condition |
| SBDSSBDS ribosome maturation factor | Rarely (1–4%) | In 1 condition |
| DCLRE1CDNA cross-link repair 1C | Not recorded | In 1 condition |
| SLC46A1solute carrier family 46 member 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.
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 2026.10.16-c6eea6bf.
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