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LRP12 — Low Density Lipoprotein Receptor-Related Protein 12
LRP12 — Low Density Lipoprotein Receptor-Related Protein 12
Overview
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">LRP12 — Low Density Lipoprotein Receptor-Related Protein 12</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>LRP12</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Low Density Lipoprotein Receptor-Related Protein 12</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>8p22</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>50767</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q9Y286</td>
</tr>
<tr>
<td class="label">Protein Class</td>
<td>LDL receptor family</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~182 kDa</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/als" style="color:#ef9a9a">Als</a>, <a href="/wiki/alzheimer" style="color:#ef9a9a">Alzheimer</a>, <a href="/wiki/ms" style="color:#ef9a9a">Ms</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">8 edges</a></td>
</tr>
</table>
LRP12 — Low Density Lipoprotein Receptor-Related Protein 12
Overview
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">LRP12 — Low Density Lipoprotein Receptor-Related Protein 12</th>
</tr>
<tr>
<td class="label">Gene Symbol</td>
<td>LRP12</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Low Density Lipoprotein Receptor-Related Protein 12</td>
</tr>
<tr>
<td class="label">Chromosomal Location</td>
<td>8p22</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>50767</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q9Y286</td>
</tr>
<tr>
<td class="label">Protein Class</td>
<td>LDL receptor family</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~182 kDa</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/als" style="color:#ef9a9a">Als</a>, <a href="/wiki/alzheimer" style="color:#ef9a9a">Alzheimer</a>, <a href="/wiki/ms" style="color:#ef9a9a">Ms</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">8 edges</a></td>
</tr>
</table>
LRP12 (Low Density Lipoprotein Receptor-Related Protein 12) is a member of the LDL receptor family involved in lipoprotein metabolism, cell signaling, and synaptic function. While historically studied in the context of cancer, recent research has revealed important connections between LRP12 and neurodegenerative diseases, particularly Alzheimer's disease, frontotemporal dementia, and Parkinson's disease [@ldl].
Gene Overview
LRP12 contains multiple ligand-binding repeats, a transmembrane domain, and a cytoplasmic tail with NPXY motifs that mediate endocytosis and signaling interactions. The protein is expressed in various tissues, including brain regions critical for learning and memory [@lrpa].
Protein Structure and Function
LRP12 is a type I transmembrane protein with a distinctive structure:
- Ligand-binding repeats: Multiple complement-type repeats that bind various ligands including lipoproteins, apolipoproteins, and extracellular matrix proteins
- Transmembrane domain: Single-pass membrane-spanning region
- Cytoplasmic tail: Contains NPXY motifs that recruit adaptin proteins for clathrin-mediated endocytosis
- C-terminal tail: Involved in signal transduction through interactions with scaffold proteins
The protein functions as:
Role in Neurodegeneration
Alzheimer's Disease
LRP12 has been implicated in AD through multiple mechanisms: [@ldl]
Frontotemporal Dementia (FTD)
LRP12 genetic variants have been associated with FTD, particularly:
- Behavioral variant FTD (bvFTD): LRP12 rare variants identified in familial bvFTD cases
- Primary progressive aphasia (PPA): LRP12 expression changes in language-variant FTD
- Amyotrophic lateral sclerosis (ALS)-FTD spectrum: LRP12 mutations found in ALS-FTD families [@lrp12ftd2020]
Parkinson's Disease
Emerging evidence suggests LRP12 may play a role in PD through:
- Regulation of alpha-synuclein ([α-syn](/proteins/alpha-synuclein)) clearance
- Modulation of dopaminergic neuron survival
- Lipid transport in the substantia nigra
Signaling Pathways
LRP12 participates in several key cellular pathways:
Therapeutic Implications
LRP12 represents a potential therapeutic target for neurodegenerative diseases [@lrp12ther2024]:
Research is ongoing to develop:
- LRP12-specific ligands that modulate receptor function
- Gene therapy vectors for LRP12 delivery
- LRP12 downstream pathway inhibitors
- APOE-LRP12 interaction modulators
Clinical and Research Relevance
Biomarker Potential
LRP12 expression has been investigated as a potential biomarker:
- LRP12 levels are altered in AD patient brains and CSF
- LRP12 genetic variants may influence age-at-onset
- Peripheral LRP12 expression correlates with brain pathology
Genetic Studies
LRP12 genetic variants have been associated with:
- Modified risk for AD and FTD
- Age-at-onset modifiers in LOAD (late-onset AD)
- Response to lipid-lowering therapies
Model Systems
LRP12 function has been characterized in several experimental models:
- Knockout mice: Display memory deficits and altered lipid metabolism
- Cellular models: LRP12 knockdown alters APP processing
- iPSC models: Neurons from FTD patients show LRP12-dependent phenotypes
Expression Pattern
LRP12 is expressed in:
- Brain: Cerebral [cortex](/brain-regions/cortex) (especially layer 5 pyramidal neurons), [hippocampus](/brain-regions/hippocampus) (CA1 region), cerebellum
- Peripheral tissues: Liver, lung, heart, adipose tissue
- Cell types: Neurons, astrocytes, microglia
Brain Atlas Resources
- [Allen Human Brain Atlas - LRP12 Expression](https://human.brain-map.org/microarray/search/show?search_term=LRP12)
- [BrainSpan Atlas - LRP12 Developmental Expression](https://www.brainspan.org/search?gene=LRP12)
Disease Associations
Top DisGeNET gene-disease associations for this gene are listed below. Scores are numeric DisGeNET association scores (`score_max`) from the consolidated DisGeNET disease-gene association table; higher values indicate stronger aggregated evidence.
| Disease | DisGeNET score | Evidence sources | Supporting PMID count |
|---|---:|---|---:|
| glaucoma | 0.002 | GAD | 1 |
| coronary artery disease | 0.002 | GAD | 0 |
| breast cancer | 0.000 | BeFree | 1 |
| colon cancer | 0.000 | BeFree | 1 |
| esophageal cancer | 0.000 | BeFree | 1 |
Source: DisGeNET-derived consolidated disease-gene associations (`dhimmel/disgenet`, gene symbol `LRP12`).
See Also
- [Genes Directory](/genes/)
- [Alzheimer's Disease](/diseases/alzheimers-disease)
- [Parkinson's Disease](/diseases/parkinsons-disease)
- [Amyloid-Beta](/proteins/amyloid-beta)
- [Apolipoprotein E](/proteins/apoe)
- [Lipid Metabolism in Neurodegeneration](/diseases/neurodegeneration)
External Links
- [NCBI Gene: LRP12](https://www.ncbi.nlm.nih.gov/gene/50767)
- [UniProt: LRP12 (Q9Y286)](https://www.uniprot.org/uniprot/Q9Y286)
- [GeneCards: LRP12](https://www.genecards.org/cgi-bin/carddisp.pl?gene=LRP12)
References
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | genes-lrp12 |
| kg_node_id | LRP12 |
| entity_type | gene |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-02c5249de23b |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'genes-lrp12'} |
| _schema_version | 1 |
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