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Trait
Glomerulonephritis
Inflammation of the renal glomeruli.
Summary
- Also called
- Glomerular nephritis
GlomerulonephritisHP:0000099
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Read the genes linked to Glomerulonephritis, and the rest of your genome, with one test.
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Get my Genome Test43 genes linked to Glomerulonephritis
Changes in these genes cause rare conditions in which Glomerulonephritis 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 |
|---|---|---|
| CD81CD81 molecule | Always | In 1 condition |
| LAMB2laminin subunit beta 2 | Always | In 1 condition |
| OAS22'-5'-oligoadenylate synthetase 2 | Always | In 1 condition |
| TAPBPTAP binding protein | Always | In 1 condition |
| WDR19WD repeat domain 19 | Always | In 1 condition |
| MMEmembrane metalloendopeptidase | Very often (80–99%) | In 1 condition |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Often (30–79%) | In 1 condition |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Often (30–79%) | In 1 condition |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Often (30–79%) | In 1 condition |
| PRTN3proteinase 3 | Often (30–79%) | In 1 condition |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Often (30–79%) | In 1 condition |
| SLC7A7solute carrier family 7 member 7 | Often (30–79%) | In 1 condition |
| ALMS1ALMS1 centrosome and basal body associated protein | Sometimes (5–29%) | In 1 condition |
| CASP10caspase 10 | Sometimes (5–29%) | In 1 condition |
| COL7A1collagen type VII alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| FASFas cell surface death receptor | Sometimes (5–29%) | In 2 conditions |
| FASLGFas ligand | Sometimes (5–29%) | In 1 condition |
| FOXP3forkhead box P3 | Sometimes (5–29%) | In 1 condition |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sometimes (5–29%) | In 1 condition |
| IL6interleukin 6 | Sometimes (5–29%) | In 1 condition |
| LACC1laccase domain multifunctional purine nucleosidase 1 | Sometimes (5–29%) | In 1 condition |
| MIFmacrophage migration inhibitory factor | Sometimes (5–29%) | In 1 condition |
| MMP1matrix metallopeptidase 1 | Sometimes (5–29%) | In 1 condition |
| SOCS1suppressor of cytokine signaling 1 | Sometimes (5–29%) | In 1 condition |
| TRIM8tripartite motif containing 8 | Sometimes (5–29%) | In 1 condition |
| C4Acomplement C4A (Chido/Rodgers blood group) | Rarely (1–4%) | In 2 conditions |
| CCR1C-C motif chemokine receptor 1 | Rarely (1–4%) | In 1 condition |
| ERAP1endoplasmic reticulum aminopeptidase 1 | Rarely (1–4%) | In 1 condition |
| HLA-Bmajor histocompatibility complex, class I, B | Rarely (1–4%) | In 1 condition |
| IFNGR1interferon gamma receptor 1 | Rarely (1–4%) | In 1 condition |
| IL10interleukin 10 | Rarely (1–4%) | In 1 condition |
| IL12Ainterleukin 12A | Rarely (1–4%) | In 1 condition |
| IL12A-AS1IL12A antisense RNA 1 | Rarely (1–4%) | In 1 condition |
| IL23Rinterleukin 23 receptor | Rarely (1–4%) | In 1 condition |
| KLRC4killer cell lectin like receptor C4 | Rarely (1–4%) | In 1 condition |
| MEFVMEFV innate immunity regulator, pyrin | Rarely (1–4%) | In 1 condition |
| STAT4signal transducer and activator of transcription 4 | Rarely (1–4%) | In 1 condition |
| TLR4toll like receptor 4 | Rarely (1–4%) | In 1 condition |
| UBAC2UBA domain containing 2 | Rarely (1–4%) | In 1 condition |
| CFHR5complement factor H related 5 | Not recorded | In 1 condition |
Show 3 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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