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Trait
Bacterial infection of skin
Clinical name: Cellulitis
A bacterial infection and inflammation of the skin und subcutaneous tissues.
Summary
- Also called
- Skin infection
- Body system
- Abnormality of the musculoskeletal system
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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/cellulitis.json"
page <- fromJSON(url)
page$trait$nameBacterial infection of skinHP:0100658
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Get my Genome Test52 genes linked to Bacterial infection of skin
Changes in these genes cause rare conditions in which Bacterial infection of skin 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 |
|---|---|---|
| COPZ1coat protein complex I subunit zeta 1 | Always | In 1 condition |
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Always | In 1 condition |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Always | In 1 condition |
| IL2RAinterleukin 2 receptor subunit alpha | Always | In 1 condition |
| MPEG1macrophage expressed 1 | Always | In 1 condition |
| PLCG2phospholipase C gamma 2 | Always | In 1 condition |
| PSTPIP1proline-serine-threonine phosphatase interacting protein 1 | Always | In 1 condition |
| SPINK5serine peptidase inhibitor Kazal type 5 | Always | In 1 condition |
| COL1A1collagen type I alpha 1 chain | Very often (80–99%) | In 1 condition |
| SLC35A1solute carrier family 35 member A1 | Very often (80–99%) | In 1 condition |
| AGGF1angiogenic factor with G-patch and FHA domains 1 | Often (30–79%) | In 1 condition |
| ARPC1Bactin related protein 2/3 complex subunit 1B | Often (30–79%) | In 1 condition |
| BTKBruton tyrosine kinase | Often (30–79%) | In 1 condition |
| EPHB4EPH receptor B4 | Often (30–79%) | In 1 condition |
| FLT4fms related receptor tyrosine kinase 4 | Often (30–79%) | In 2 conditions |
| FOXC2forkhead box C2 | Often (30–79%) | In 1 condition |
| IL6Rinterleukin 6 receptor | Often (30–79%) | In 1 condition |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Often (30–79%) | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Often (30–79%) | In 1 condition |
| RAC2Rac family small GTPase 2 | Often (30–79%) | In 1 condition |
| RFX5regulatory factor X5 | Often (30–79%) | In 1 condition |
| AEBP1AE binding protein 1 | Sometimes (5–29%) | In 2 conditions |
| BLNKB cell linker | Sometimes (5–29%) | In 1 condition |
| CD79ACD79a molecule | Sometimes (5–29%) | In 1 condition |
| CD79BCD79b molecule | Sometimes (5–29%) | In 1 condition |
| CLPBClpB family mitochondrial disaggregase | Sometimes (5–29%) | In 1 condition |
| ELANEelastase, neutrophil expressed | Sometimes (5–29%) | In 2 conditions |
| GFI1growth factor independent 1 transcriptional repressor | Sometimes (5–29%) | In 1 condition |
| GJC2gap junction protein gamma 2 | Sometimes (5–29%) | In 2 conditions |
| IGHMimmunoglobulin heavy constant mu | Sometimes (5–29%) | In 1 condition |
| IGLL1immunoglobulin lambda like polypeptide 1 | Sometimes (5–29%) | In 1 condition |
| KIF11kinesin family member 11 | Sometimes (5–29%) | In 1 condition |
| LMNAlamin A/C | Sometimes (5–29%) | In 1 condition |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | Sometimes (5–29%) | In 1 condition |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Sometimes (5–29%) | In 2 conditions |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sometimes (5–29%) | In 1 condition |
| SHANK3SH3 and multiple ankyrin repeat domains 3 | Sometimes (5–29%) | In 1 condition |
| SPI1Spi-1 proto-oncogene | Sometimes (5–29%) | In 1 condition |
| SRP19signal recognition particle 19 | Sometimes (5–29%) | In 1 condition |
| STAT3signal transducer and activator of transcription 3 | Sometimes (5–29%) | In 1 condition |
Show 12 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| TCF3transcription factor 3 | Sometimes (5–29%) | In 1 condition |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Sometimes (5–29%) | In 1 condition |
| TNFRSF1ATNF receptor superfamily member 1A | Sometimes (5–29%) | In 1 condition |
| VEGFCvascular endothelial growth factor C | Sometimes (5–29%) | In 1 condition |
| CXCR4C-X-C motif chemokine receptor 4 | Rarely (1–4%) | In 1 condition |
| PHEXphosphate regulating endopeptidase X-linked | Rarely (1–4%) | In 1 condition |
| CYBAcytochrome b-245 alpha chain | Not recorded | In 1 condition |
| CYBBcytochrome b-245 beta chain | Not recorded | In 1 condition |
| GATA2GATA binding protein 2 | Not recorded | In 1 condition |
| NCF1neutrophil cytosolic factor 1 | Not recorded | In 1 condition |
| NCF2neutrophil cytosolic factor 2 | Not recorded | In 1 condition |
| SLC35C1solute carrier family 35 member C1 | 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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