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TREM2 Gene
TREM2 — Triggering Receptor Expressed on Myeloid Cells 2
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">TREM2 Gene</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>TREM2</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Triggering Receptor Expressed on Myeloid Cells 2</td>
</tr>
<tr>
<td class="label">Aliases</td>
<td>TREM-2, PLOSL, CSF-1</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>6p21.1</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>54206</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q9NZC2</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000160310</td>
</tr>
<tr>
<td class="label">OMIM ID</td>
<td>605086</td>
</tr>
<tr>
<td class="label">Gene Type</td>
<td>Protein Coding</td>
</tr>
<tr>
<td class="label">Gene Length</td>
<td>~3.3 kb</td>
</tr>
<tr>
<td class="label">Transcript Length</td>
<td>~0.9 kb</td>
</tr>
<tr>
<td class="label">Tissue</td>
<td>Expression Level</td>
</tr>
<tr>
<td class="label">Brain</td>
<td>Highest</td>
</tr>
<tr>
<td class="label">Bone marrow</td>
<td>High</td>
</tr>
<tr>
<td class="label">Lung</td>
<td>Moderate</td>
</tr>
<tr>
<td class="label">Liver</td>
<td>Moderate</td>
</tr>
<tr>
<td class="label">Spleen</td>
<td>Moderate</td>
</tr>
<tr>
<td class="label">Approach</td>
<td>Description</td>
</tr>
<tr>
<td class="label">Anti-T
TREM2 — Triggering Receptor Expressed on Myeloid Cells 2
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">TREM2 Gene</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>TREM2</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Triggering Receptor Expressed on Myeloid Cells 2</td>
</tr>
<tr>
<td class="label">Aliases</td>
<td>TREM-2, PLOSL, CSF-1</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>6p21.1</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>54206</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q9NZC2</td>
</tr>
<tr>
<td class="label">Ensembl ID</td>
<td>ENSG00000160310</td>
</tr>
<tr>
<td class="label">OMIM ID</td>
<td>605086</td>
</tr>
<tr>
<td class="label">Gene Type</td>
<td>Protein Coding</td>
</tr>
<tr>
<td class="label">Gene Length</td>
<td>~3.3 kb</td>
</tr>
<tr>
<td class="label">Transcript Length</td>
<td>~0.9 kb</td>
</tr>
<tr>
<td class="label">Tissue</td>
<td>Expression Level</td>
</tr>
<tr>
<td class="label">Brain</td>
<td>Highest</td>
</tr>
<tr>
<td class="label">Bone marrow</td>
<td>High</td>
</tr>
<tr>
<td class="label">Lung</td>
<td>Moderate</td>
</tr>
<tr>
<td class="label">Liver</td>
<td>Moderate</td>
</tr>
<tr>
<td class="label">Spleen</td>
<td>Moderate</td>
</tr>
<tr>
<td class="label">Approach</td>
<td>Description</td>
</tr>
<tr>
<td class="label">Anti-TREM2 antibodies</td>
<td>Agonist antibodies to enhance function</td>
</tr>
<tr>
<td class="label">TREM2 agonists</td>
<td>Small molecule activators</td>
</tr>
<tr>
<td class="label">Gene therapy</td>
<td>Restore TREM2 expression</td>
</tr>
<tr>
<td class="label">sTREM2 replacement</td>
<td>Soluble TREM2 protein</td>
</tr>
</table>
Overview
TREM2 (Triggering Receptor Expressed on Myeloid Cells 2) encodes a cell surface receptor expressed primarily on microglia in the brain[@guerreiro2013]. It is one of the strongest genetic risk factors for [Alzheimer's disease](/diseases/alzheimers-disease), with common variants increasing AD risk approximately 3-4 fold. Rare loss-of-function variants cause a syndrome called Nasu-Hakola disease (polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy, PLOSL), characterized by early-onset dementia and bone cysts. PMID: 39241780
TREM2 is a member of the immunoglobulin superfamily and acts as an innate immune receptor that recognizes lipid components, ApoE, and other ligands. It triggers intracellular signaling through the adaptor protein DAP12 (TYROBP), leading to microglial activation, phagocytosis, and inflammatory responses. The discovery of TREM2's role in AD has revolutionized our understanding of microglial contributions to neurodegeneration. PMID: 39475571
Gene Information
Protein Structure
TREM2 is a 231-amino acid type I transmembrane protein with distinctive domains[@guerreiro2013]: PMID: 26250687
- Signal peptide (1-18): Directs protein to secretory pathway
- Immunoglobulin-like V-type domain (19-167):
- Extracellular ligand-binding domain
- Contains conserved disulfide bond
- Multiple ligand interactions
- Transmembrane domain (168-200): Single membrane-spanning helix PMID: 29874566
- Cytoplasmic tail (201-231):
- Short cytoplasmic domain
- Associates with DAP12 adaptor via transmembrane domain
The TREM2-DAP12 complex triggers signaling through SYK and other kinases. PMID: 32755557
Biological Functions
Microglial Phagocytosis
TREM2 is critical for microglial phagocytosis[@ulrich2016]:
- Recognizes apoptotic cell remnants
- Triggers engulfment of cellular debris
- Essential for amyloid plaque clearance
- Loss of function leads to defective phagocytosis
Lipid Metabolism
TREM2 recognizes lipid components:
- Binds to lipoproteins (LDL, VLDL)
- Recognizes phospholipids on apoptotic cells
- Interacts with ApoE (lipid carrier)
- May sense cellular stress through lipid changes
Microglial Activation
TREM2 modulates microglial inflammatory responses:
- Triggers pro-inflammatory signaling
- May have both activating and regulatory roles
- Links innate immunity to neurodegeneration
- DAP12-dependent signaling cascade
Cell Survival
TREM2 promotes microglial survival:
- Anti-apoptotic signaling through DAP12
- Supports microglial proliferation
- May protect against cell death
Expression Pattern
Tissue Distribution
TREM2 is expressed predominantly in myeloid cells[@guerreiro2013]:
Brain Expression
In the brain, TREM2 is almost exclusively expressed in microglia:
- Activated microglia: Highest expression around amyloid plaques
- Rama/amoeboid microglia: High in developing brain
- Disease-associated microglia (DAM): Upregulated in AD
- Minimal expression: In neurons, astrocytes, oligodendrocytes
Subcellular Localization
- Plasma membrane: Primary location
- Phagosomes: Present after phagocytosis
- Soluble form (sTREM2): Shed from membrane (proteolytic cleavage)
Role in Alzheimer's Disease
Genetic Evidence
TREM2 variants are strong genetic risk factors for late-onset AD[@guerreiro2013]:
- Common variants (R47H, R62H): ~3-4x increased AD risk
- Rare variants: Cause Nasu-Hakola disease (PLOSL)
- Protective variants: Some rare variants reduce risk
- GWAS significance: One of the strongest AD risk loci
AD Risk Variants
The TREM2 R47H variant (rs75932628) is strongly associated with AD:
- Odds ratio: ~3.5 for heterozygous carriers
- Population frequency: ~0.1% in Europeans
- Mechanism: Impaired ligand binding
- Similar to R62H: Also increases risk (~2-3x)
Pathogenic Mechanisms
TREM2 variants contribute to AD through multiple mechanisms[@ulrich2016]:
Microglial Dysfunction
TREM2 mutations affect microglial function in AD:
- Plaque-associated microglia: Reduced clustering around plaques
- Phagocytic capacity: Impaired debris clearance
- Inflammatory milieu: Altered cytokine profiles
- Neurotoxicity: May contribute to neuronal loss
Therapeutic Implications
TREM2 Targeting
TREM2 is a promising therapeutic target for AD[@ulrich2016]:
Antibody Approaches
- Anti-TREM2 antibodies: Activate signaling (like ligand binding)
- Alzhemed: Originally developed as TREM2 agonist
- Pepinemab (AL003): Anti-TREM2 antibody in trials
Small Molecule Modulators
- TREM2-binding small molecules
- DAP12 pathway modulators
- SYK inhibitors
Cross-Links
- [Alzheimer's Disease](/diseases/alzheimers-disease) — AD overview
- [Microglia](/entities/microglia) — Immune cells
- [APP Gene](/entities/app) — APP (amyloid)
- [APOE Gene](/entities/apoe) — APOE (AD risk factor)
- [Tau Protein](/proteins/tau-protein) — Tau pathology
- [Nasu-Hakola Disease](/diseases/nasu-hakola-disease) — TREM2 loss-of-function
References
Related Hypotheses
From the [SciDEX Exchange](/exchange) — scored by multi-agent debate
- [TREM2-mediated microglial tau clearance enhancement](/hypothesis/h-b234254c) — <span style="color:#ffd54f;font-weight:600">0.52</span> · Target: TREM2
- [TREM2 Conformational Stabilizers for Synaptic Discrimination](/hypothesis/h-044ee057) — <span style="color:#ff8a65;font-weight:600">0.40</span> · Target: TREM2
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | entities-trem2 |
| kg_node_id | None |
| entity_type | gene |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-ceaecfe17e20 |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'entities-trem2'} |
| _schema_version | 1 |
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