Trait
Meningitis
Inflammation of the meninges.
Summary
- Also called
- Unusual infectious meningitis, Unusual meningitis
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test82 genes linked to Meningitis
Changes in these genes cause rare conditions in which Meningitis 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 |
| DCLRE1CDNA cross-link repair 1C | Always | In 1 condition |
| FDXRferredoxin reductase | Always | In 1 condition |
| IRAK4interleukin 1 receptor associated kinase 4 | Always | In 1 condition |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Always | In 1 condition |
| MRTFAmyocardin related transcription factor A | Always | In 1 condition |
| NOTCH3notch receptor 3 | Always | In 1 condition |
| RAG1recombination activating 1 | Always | In 2 conditions |
| RAG2recombination activating 2 | Always | In 2 conditions |
| SPINK5serine peptidase inhibitor Kazal type 5 | Always | In 1 condition |
| TLR3toll like receptor 3 | Always | In 1 condition |
| TOP2BDNA topoisomerase II beta | Always | In 1 condition |
| C4Acomplement C4A (Chido/Rodgers blood group) | Very often (80–99%) | In 1 condition |
| 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 2 conditions |
| IFNGR1interferon gamma receptor 1 | Very often (80–99%) | In 1 condition |
| IL10interleukin 10 | Very often (80–99%) | In 1 condition |
| 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 3 conditions |
| NLRP3NLR family pyrin domain containing 3 | Very often (80–99%) | In 2 conditions |
| STAT4signal transducer and activator of transcription 4 | 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 |
| ARPC1Bactin related protein 2/3 complex subunit 1B | Often (30–79%) | In 1 condition |
| BTKBruton tyrosine kinase | Often (30–79%) | In 3 conditions |
| NDE1nudE neurodevelopment protein 1 | Often (30–79%) | In 1 condition |
| NLRC4NLR family CARD domain containing 4 | Often (30–79%) | In 1 condition |
| BCL2BCL2 apoptosis regulator | Sometimes (5–29%) | In 1 condition |
| BCL6BCL6 transcription repressor | Sometimes (5–29%) | In 1 condition |
| BLNKB cell linker | Sometimes (5–29%) | In 1 condition |
| CARD9caspase recruitment domain family member 9 | Sometimes (5–29%) | In 1 condition |
| CD40LGCD40 ligand | Sometimes (5–29%) | In 1 condition |
| CD79ACD79a molecule | Sometimes (5–29%) | In 1 condition |
| CD79BCD79b molecule | Sometimes (5–29%) | In 1 condition |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Sometimes (5–29%) | In 1 condition |
Show 42 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| CYBAcytochrome b-245 alpha chain | Sometimes (5–29%) | In 1 condition |
| CYBBcytochrome b-245 beta chain | Sometimes (5–29%) | In 1 condition |
| CYBC1cytochrome b-245 chaperone 1 | Sometimes (5–29%) | In 1 condition |
| DNASE1L3deoxyribonuclease 1L3 | Sometimes (5–29%) | In 1 condition |
| FCGR3BFc gamma receptor IIIb | Sometimes (5–29%) | In 1 condition |
| FOXN1forkhead box N1 | Sometimes (5–29%) | In 1 condition |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Sometimes (5–29%) | In 1 condition |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Sometimes (5–29%) | In 1 condition |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sometimes (5–29%) | In 2 conditions |
| IGHimmunoglobulin heavy locus | Sometimes (5–29%) | In 1 condition |
| IGHMimmunoglobulin heavy constant mu | Sometimes (5–29%) | In 1 condition |
| IGLL1immunoglobulin lambda like polypeptide 1 | Sometimes (5–29%) | In 2 conditions |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | Sometimes (5–29%) | In 1 condition |
| NCF1neutrophil cytosolic factor 1 | Sometimes (5–29%) | In 1 condition |
| NCF2neutrophil cytosolic factor 2 | Sometimes (5–29%) | In 1 condition |
| NCF4neutrophil cytosolic factor 4 | Sometimes (5–29%) | In 1 condition |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Sometimes (5–29%) | In 1 condition |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Sometimes (5–29%) | In 1 condition |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sometimes (5–29%) | In 1 condition |
| PRTN3proteinase 3 | Sometimes (5–29%) | In 1 condition |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Sometimes (5–29%) | In 2 conditions |
| SH2D1ASH2 domain containing 1A | Sometimes (5–29%) | In 1 condition |
| SPI1Spi-1 proto-oncogene | Sometimes (5–29%) | In 2 conditions |
| TCF3transcription factor 3 | Sometimes (5–29%) | In 1 condition |
| TFRCtransferrin receptor | Sometimes (5–29%) | In 1 condition |
| WASWASP actin nucleation promoting factor | Sometimes (5–29%) | In 1 condition |
| XIAPX-linked inhibitor of apoptosis | Sometimes (5–29%) | In 1 condition |
| CXCR4C-X-C motif chemokine receptor 4 | Rarely (1–4%) | In 1 condition |
| FOXP3forkhead box P3 | Rarely (1–4%) | In 1 condition |
| MNX1motor neuron and pancreas homeobox 1 | Rarely (1–4%) | In 1 condition |
| C8Acomplement C8 alpha chain | Not recorded | In 1 condition |
| C8Bcomplement C8 beta chain | Not recorded | In 1 condition |
| CD19CD19 molecule | Not recorded | In 1 condition |
| CFBcomplement factor B | Not recorded | In 1 condition |
| CR2complement C3d receptor 2 | Not recorded | In 1 condition |
| ICOSinducible T cell costimulator | Not recorded | In 1 condition |
| JAK3Janus kinase 3 | Not recorded | In 1 condition |
| PRF1perforin 1 | Not recorded | In 1 condition |
| TBK1TANK binding kinase 1 | Not recorded | In 1 condition |
| TNFRSF13BTNF receptor superfamily member 13B | Not recorded | In 1 condition |
| TNFRSF13CTNF receptor superfamily member 13C | Not recorded | In 1 condition |
| VANGL1VANGL planar cell polarity protein 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.
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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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