Trait
Redness of skin or mucous membrane
Clinical name: Erythema
Redness of the skin, caused by hyperemia of the capillaries in the lower layers of the skin.
Summary
Reference genomeGRCh38hg38
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Read the genes linked to Redness of skin or mucous membrane, and the rest of your genome, with one test.
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Get my Genome Test127 genes linked to Redness of skin or mucous membrane
Changes in these genes cause rare conditions in which Redness of skin or mucous membrane 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 |
|---|---|---|
| CD40LGCD40 ligand | Always | In 1 condition |
| DBR1debranching RNA lariats 1 | Always | In 1 condition |
| DCLRE1CDNA cross-link repair 1C | Always | In 1 condition |
| ELOVL4ELOVL fatty acid elongase 4 | Always | In 1 condition |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Always | In 2 conditions |
| GJA1gap junction protein alpha 1 | Always | In 2 conditions |
| GJB4gap junction protein beta 4 | Always | In 2 conditions |
| GTF2H4general transcription factor IIH subunit 4 | Always | In 1 condition |
| IRF4interferon regulatory factor 4 | Always | In 1 condition |
| KDSR3-ketodihydrosphingosine reductase | Always | In 3 conditions |
| KLK11kallikrein related peptidase 11 | Always | In 1 condition |
| KRT1keratin 1 | Always | In 2 conditions |
| KRT10keratin 10 | Always | In 1 condition |
| LRP1LDL receptor related protein 1 | Always | In 2 conditions |
| LYNLYN proto-oncogene, Src family tyrosine kinase | Always | In 1 condition |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Always | In 1 condition |
| OTULINOTU deubiquitinase with linear linkage specificity | Always | In 1 condition |
| PLCG2phospholipase C gamma 2 | Always | In 2 conditions |
| PSMG2proteasome assembly chaperone 2 | Always | In 1 condition |
| RAG1recombination activating 1 | Always | In 1 condition |
| RAG2recombination activating 2 | Always | In 1 condition |
| SPINK5serine peptidase inhibitor Kazal type 5 | Always | In 2 conditions |
| SULT2B1sulfotransferase family 2B member 1 | Always | In 1 condition |
| TGM5transglutaminase 5 | Always | In 2 conditions |
| TREX1three prime repair exonuclease 1 | Always | In 1 condition |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Very often (80–99%) | In 1 condition |
| ATP2C1ATPase secretory pathway Ca2+ transporting 1 | Very often (80–99%) | In 2 conditions |
| CD28CD28 molecule | Very often (80–99%) | In 1 condition |
| CLEC7AC-type lectin domain containing 7A | Very often (80–99%) | In 1 condition |
| COL1A1collagen type I alpha 1 chain | Very often (80–99%) | In 1 condition |
| COX7Bcytochrome c oxidase subunit 7B | Very often (80–99%) | In 1 condition |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Very often (80–99%) | In 1 condition |
| CTSBcathepsin B | Very often (80–99%) | In 2 conditions |
| FECHferrochelatase | Very often (80–99%) | In 2 conditions |
| FERMT1FERM domain containing kindlin 1 | Very often (80–99%) | In 1 condition |
| GJB3gap junction protein beta 3 | Very often (80–99%) | In 1 condition |
| HCCSholocytochrome c synthase | Very often (80–99%) | In 1 condition |
| HLA-Bmajor histocompatibility complex, class I, B | Very often (80–99%) | In 1 condition |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Very often (80–99%) | In 1 condition |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Very often (80–99%) | In 1 condition |
Show 87 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Very often (80–99%) | In 2 conditions |
| IKZF1IKAROS family zinc finger 1 | Very often (80–99%) | In 1 condition |
| IL17Finterleukin 17F | Very often (80–99%) | In 1 condition |
| IL17RAinterleukin 17 receptor A | Very often (80–99%) | In 1 condition |
| IL17RCinterleukin 17 receptor C | Very often (80–99%) | In 1 condition |
| KRT14keratin 14 | Very often (80–99%) | In 1 condition |
| KRT5keratin 5 | Very often (80–99%) | In 1 condition |
| KRT83keratin 83 | Very often (80–99%) | In 1 condition |
| LORICRINloricrin cornified envelope precursor protein | Very often (80–99%) | In 1 condition |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Very often (80–99%) | In 2 conditions |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Very often (80–99%) | In 1 condition |
| NLRP3NLR family pyrin domain containing 3 | Very often (80–99%) | In 1 condition |
| NOD2nucleotide binding oligomerization domain containing 2 | Very often (80–99%) | In 1 condition |
| PDGFBplatelet derived growth factor subunit B | Very often (80–99%) | In 1 condition |
| PEPDpeptidase D | Very often (80–99%) | In 1 condition |
| PERPp53 apoptosis effector related to PMP22 | Very often (80–99%) | In 1 condition |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Very often (80–99%) | In 1 condition |
| RECQL4RecQ like helicase 4 | Very often (80–99%) | In 2 conditions |
| SCN10Asodium voltage-gated channel alpha subunit 10 | Very often (80–99%) | In 1 condition |
| SCN11Asodium voltage-gated channel alpha subunit 11 | Very often (80–99%) | In 1 condition |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Very often (80–99%) | In 1 condition |
| SLC39A4solute carrier family 39 member 4 | Very often (80–99%) | In 1 condition |
| TGM1transglutaminase 1 | Very often (80–99%) | In 1 condition |
| TNFRSF1BTNF receptor superfamily member 1B | Very often (80–99%) | In 1 condition |
| TRAF3IP2TRAF3 interacting protein 2 | Very often (80–99%) | In 1 condition |
| TRPM4transient receptor potential cation channel subfamily M member 4 | Very often (80–99%) | In 1 condition |
| TRPV3transient receptor potential cation channel subfamily V member 3 | Very often (80–99%) | In 1 condition |
| ADAM17ADAM metallopeptidase domain 17 | Often (30–79%) | In 1 condition |
| AP1S1adaptor related protein complex 1 subunit sigma 1 | Often (30–79%) | In 1 condition |
| AQP5aquaporin 5 | Often (30–79%) | In 1 condition |
| COL7A1collagen type VII alpha 1 chain | Often (30–79%) | In 1 condition |
| CSTAcystatin A | Often (30–79%) | In 1 condition |
| DDB2damage specific DNA binding protein 2 | Often (30–79%) | In 1 condition |
| DSTdystonin | Often (30–79%) | In 1 condition |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Often (30–79%) | In 1 condition |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Often (30–79%) | In 1 condition |
| ERCC5ERCC excision repair 5, endonuclease | Often (30–79%) | In 1 condition |
| GLULglutamate-ammonia ligase | Often (30–79%) | In 1 condition |
| LIG4DNA ligase 4 | Often (30–79%) | In 1 condition |
| MEFVMEFV innate immunity regulator, pyrin | Often (30–79%) | In 2 conditions |
| PORCNporcupine O-acyltransferase | Often (30–79%) | In 1 condition |
| SLURP1secreted LY6/PLAUR domain containing 1 | Often (30–79%) | In 1 condition |
| TNFRSF1ATNF receptor superfamily member 1A | Often (30–79%) | In 1 condition |
| XPAXPA, DNA damage recognition and repair factor | Often (30–79%) | In 1 condition |
| XPCXPC complex subunit, DNA damage recognition and repair factor | Often (30–79%) | In 1 condition |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Sometimes (5–29%) | In 1 condition |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Sometimes (5–29%) | In 2 conditions |
| BMS1BMS1 ribosome biogenesis factor | Sometimes (5–29%) | In 1 condition |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Sometimes (5–29%) | In 1 condition |
| DLL4delta like canonical Notch ligand 4 | Sometimes (5–29%) | In 1 condition |
| DSG4desmoglein 4 | Sometimes (5–29%) | In 1 condition |
| GNB2G protein subunit beta 2 | Sometimes (5–29%) | In 1 condition |
| ITGB4integrin subunit beta 4 | Sometimes (5–29%) | In 1 condition |
| KITKIT proto-oncogene, receptor tyrosine kinase | Sometimes (5–29%) | In 2 conditions |
| KRT2keratin 2 | Sometimes (5–29%) | In 1 condition |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Sometimes (5–29%) | In 1 condition |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Sometimes (5–29%) | In 1 condition |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Sometimes (5–29%) | In 1 condition |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Sometimes (5–29%) | In 1 condition |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Sometimes (5–29%) | In 1 condition |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Sometimes (5–29%) | In 1 condition |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Sometimes (5–29%) | In 1 condition |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Sometimes (5–29%) | In 1 condition |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Sometimes (5–29%) | In 1 condition |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Sometimes (5–29%) | In 1 condition |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Sometimes (5–29%) | In 1 condition |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Sometimes (5–29%) | In 1 condition |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Sometimes (5–29%) | In 1 condition |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Sometimes (5–29%) | In 1 condition |
| MVKmevalonate kinase | Sometimes (5–29%) | In 1 condition |
| NAXDNAD(P)HX dehydratase | Sometimes (5–29%) | In 1 condition |
| PGM3phosphoglucomutase 3 | Sometimes (5–29%) | In 1 condition |
| PLECplectin | Sometimes (5–29%) | In 1 condition |
| RNF168ring finger protein 168 | Sometimes (5–29%) | In 1 condition |
| UBA2ubiquitin like modifier activating enzyme 2 | Sometimes (5–29%) | In 1 condition |
| XPNPEP2X-prolyl aminopeptidase 2 | Sometimes (5–29%) | In 1 condition |
| DDR2discoidin domain receptor tyrosine kinase 2 | Not recorded | In 1 condition |
| DSPdesmoplakin | Not recorded | In 1 condition |
| HPGD15-hydroxyprostaglandin dehydrogenase | Not recorded | In 1 condition |
| IL36RNinterleukin 36 receptor antagonist | Not recorded | In 1 condition |
| ITGA3integrin subunit alpha 3 | Not recorded | In 1 condition |
| LIPNlipase family member N | Not recorded | In 1 condition |
| PSMB8proteasome 20S subunit beta 8 | Not recorded | In 1 condition |
| SERPING1serpin family G member 1 | Not recorded | In 1 condition |
| STAT3signal transducer and activator of transcription 3 | Not recorded | In 1 condition |
| STING1stimulator of interferon response cGAMP interactor 1 | Not recorded | In 1 condition |
| WNT10AWnt family member 10A | 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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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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