Trait
Pyelonephritis
An inflammation of the kidney involving the parenchyma of kidney, the renal pelvis and the kidney calices.
Summary
Reference genomeGRCh38hg38
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Read the genes linked to Pyelonephritis, and the rest of your genome, with one test.
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Get my Genome Test24 genes linked to Pyelonephritis
Changes in these genes cause rare conditions in which Pyelonephritis 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 |
|---|---|---|
| CHASERRCHD2 adjacent suppressive regulatory RNA | Always | In 1 condition |
| HOXA13homeobox A13 | Always | In 1 condition |
| MYH11myosin heavy chain 11 | Always | In 1 condition |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Always | In 1 condition |
| ZMYM3zinc finger MYM-type containing 3 | Always | In 1 condition |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Sometimes (5–29%) | In 1 condition |
| ALG5ALG5 dolichyl-phosphate beta-glucosyltransferase | Sometimes (5–29%) | In 1 condition |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Sometimes (5–29%) | In 1 condition |
| BICC1BicC family RNA binding protein 1 | Sometimes (5–29%) | In 1 condition |
| BNC2basonuclin zinc finger protein 2 | Sometimes (5–29%) | In 1 condition |
| DNAJB11DnaJ heat shock protein family (Hsp40) member B11 | Sometimes (5–29%) | In 1 condition |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Sometimes (5–29%) | In 1 condition |
| ELNelastin | Sometimes (5–29%) | In 1 condition |
| FBLN5fibulin 5 | Sometimes (5–29%) | In 2 conditions |
| GANABglucosidase II alpha subunit | Sometimes (5–29%) | In 1 condition |
| IFT140intraflagellar transport 140 | Sometimes (5–29%) | In 1 condition |
| KCTD1potassium channel tetramerization domain containing 1 | Sometimes (5–29%) | In 2 conditions |
| LTBP1latent transforming growth factor beta binding protein 1 | Sometimes (5–29%) | In 1 condition |
| MED12mediator complex subunit 12 | Sometimes (5–29%) | In 1 condition |
| NEK8NIMA related kinase 8 | Sometimes (5–29%) | In 1 condition |
| PKD1polycystin 1, transient receptor potential channel interacting | Sometimes (5–29%) | In 1 condition |
| PKD2polycystin 2, transient receptor potential cation channel | Sometimes (5–29%) | In 1 condition |
| CFIcomplement factor I | Not recorded | In 1 condition |
| XDHxanthine dehydrogenase | 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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