Alzheimer disease 18
diseaseOn this page
Also known as AD18ADAM10 Alzheimer diseaseAlzheimer disease caused by mutation in ADAM10Alzheimer disease type 18Alzheimer's disease 18Alzheimer's disease type 18
Summary
Alzheimer disease 18 (MONDO:0014265) is a disease with 1 cohort gene and 2 clinical trials.
At a glance
- Cohort genes: 1
- ClinVar variants: 3
- Clinical trials: 2
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | Alzheimer disease 18 |
| Mondo ID | MONDO:0014265 |
| OMIM | 615590 |
| DOID | DOID:0110050 |
| UMLS | C3810041 |
| MedGen | 816371 |
| GARD | 0024982 |
| Is cancer (heuristic) | no |
Also known as: AD18 · ADAM10 Alzheimer disease · Alzheimer disease 18 · Alzheimer disease caused by mutation in ADAM10 · Alzheimer disease type 18 · Alzheimer’s disease 18 · Alzheimer’s disease type 18
Data availability: 3 ClinVar variants · 6 cell lines.
Disease family
Classification path: disease › human disease › disease by developmental or physiological process › psychiatric disorder › cognitive disorder › dementia › Alzheimer disease › Alzheimer disease 18
Related subtypes (4): Alzheimer disease 16, Alzheimer disease 17, Alzheimer disease 19, familial Alzheimer disease
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
ClinVar germline variants
3 retrieved; paginated sample, class counts are floors:
1 benign/likely benign, 1 uncertain significance, 1 risk factor
| ClinVar | Variant (HGVS) | Gene | Classification | Review |
|---|---|---|---|---|
| 92164 | NM_001110.4(ADAM10):c.541A>G (p.Arg181Gly) | ADAM10 | risk factor | no assertion criteria provided |
| 92163 | NM_001110.4(ADAM10):c.510G>C (p.Gln170His) | ADAM10 | Uncertain significance | criteria provided, multiple submitters, no conflicts |
| 720402 | NM_001110.4(ADAM10):c.326-10T>C | ADAM10 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts |
Genes & proteins
Mendelian disease overlap and somatic drivers
GenCC: 0 · Orphanet: 1 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0
Orphanet rare-disease linkage (cohort genes)
| Gene | Orphanet ID | Rare disease |
|---|---|---|
| ADAM10 | Orphanet:178307 | Reticulate acropigmentation of Kitamura |
Cohort genes → proteins
1 cohort genes, 1 distinct canonical proteins.
Evidence partition
| Subset | Genes |
|---|---|
| multi_evidence | 1 |
Cohort genes (full)
| Symbol | HGNC | Ensembl | UniProt | Name | Evidence |
|---|---|---|---|---|---|
| ADAM10 | HGNC:188 | ENSG00000137845 | O14672 | Disintegrin and metalloproteinase domain-containing protein 10 | clinvar |
Cohort function summary
Lead sentence per gene, UniProt-curated.
| Symbol | Protein name | Function (lead sentence) |
|---|---|---|
| ADAM10 | Disintegrin and metalloproteinase domain-containing protein 10 | Transmembrane metalloprotease which mediates the ectodomain shedding of a myriad of transmembrane proteins, including adhesion proteins, growth factor precursors and cytokines being essential for development and tissue homeostasis. |
Protein-family classification
Druggable: 1 · Difficult: 0 · Unknown: 0 · Druggable fraction: 1.0
Family distribution
Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.
| Family | Genes | Fold | FDR |
|---|---|---|---|
| Protease | 1 | 36.6× | 0.027 |
Per-gene assignment
| Symbol | Family | Druggable? | EC | InterPro (top 3) |
|---|---|---|---|---|
| ADAM10 | Protease | yes | 3.4.24.81 | Peptidase_M12B, Disintegrin_dom, MetalloPept_cat_dom_sf |
Expression context
Cohort genes with no expression data: 0.
1 cohort gene are a single-cell marker in ≥1 SCXA experiment.
Breadth distribution (Bgee present_calls)
| Bucket | Genes |
|---|---|
| narrow (1-5 tissues) | 0 |
| moderate (6-20) | 0 |
| broad (>20) | 1 |
| unknown | 0 |
Top tissues across cohort
| Tissue | Cohort genes |
|---|---|
| amniotic fluid | 1 |
| stromal cell of endometrium | 1 |
| trigeminal ganglion | 1 |
Per-gene tissue summary (top 30)
| Symbol | Bgee breadth | FANTOM5 breadth | SCXA | Top tissues |
|---|---|---|---|---|
| ADAM10 | 298 | ubiquitous | marker | stromal cell of endometrium, amniotic fluid, trigeminal ganglion |
Protein interactions among cohort
Intra-cohort edges: 0.
Hub genes (top 10 by interactor count)
| Symbol | Interactor count |
|---|---|
| ADAM10 | 3,603 |
Structural data
PDB: 1 · AlphaFold-only: 0 · No structure: 0
Cohort genes with PDB structures (top 30)
| Symbol | UniProt | PDB entries |
|---|---|---|
| ADAM10 | O14672 | 3 |
Function
Pathway analysis
Distinct Reactome pathways touched by cohort: 39. Enrichment computed across 1 evidence-associated genes (1 with Reactome annotation).
Pathways by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| Pathway | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| Signaling by NOTCH1 t(7;9)(NOTCH1:M1580_K2555) Translocation Mutant | 1 | 2855.0× | 0.007 | ADAM10 |
| Constitutive Signaling by NOTCH1 t(7;9)(NOTCH1:M1580_K2555) Translocation Mutant | 1 | 1631.4× | 0.007 | ADAM10 |
| Signaling by NOTCH1 HD Domain Mutants in Cancer | 1 | 1268.9× | 0.007 | ADAM10 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | 1 | 1038.2× | 0.007 | ADAM10 |
| Constitutive Signaling by NOTCH1 HD Domain Mutants | 1 | 761.3× | 0.007 | ADAM10 |
| Signaling by NOTCH2 | 1 | 713.8× | 0.007 | ADAM10 |
| Signaling by NOTCH3 | 1 | 519.1× | 0.007 | ADAM10 |
| Signaling by NOTCH4 | 1 | 496.5× | 0.007 | ADAM10 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 1 | 475.8× | 0.007 | ADAM10 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 1 | 439.2× | 0.007 | ADAM10 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 1 | 407.9× | 0.007 | ADAM10 |
| Signaling by NOTCH1 in Cancer | 1 | 407.9× | 0.007 | ADAM10 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 1 | 407.9× | 0.007 | ADAM10 |
| Signaling by NOTCH1 | 1 | 356.9× | 0.007 | ADAM10 |
| Activated NOTCH1 Transmits Signal to the Nucleus | 1 | 356.9× | 0.007 | ADAM10 |
| Signaling by EGFR | 1 | 326.3× | 0.007 | ADAM10 |
| EPH-ephrin mediated repulsion of cells | 1 | 219.6× | 0.010 | ADAM10 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 1 | 196.9× | 0.010 | ADAM10 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 1 | 196.9× | 0.010 | ADAM10 |
| Collagen degradation | 1 | 175.7× | 0.011 | ADAM10 |
| Signaling by NOTCH | 1 | 175.7× | 0.011 | ADAM10 |
| EPH-Ephrin signaling | 1 | 165.5× | 0.011 | ADAM10 |
| Degradation of the extracellular matrix | 1 | 117.7× | 0.014 | ADAM10 |
| Amyloid fiber formation | 1 | 102.9× | 0.016 | ADAM10 |
| Post-translational protein phosphorylation | 1 | 100.2× | 0.016 | ADAM10 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 1 | 86.5× | 0.017 | ADAM10 |
| Extracellular matrix organization | 1 | 63.1× | 0.023 | ADAM10 |
| Diseases of signal transduction by growth factor receptors and second messengers | 1 | 56.8× | 0.025 | ADAM10 |
| Signaling by Receptor Tyrosine Kinases | 1 | 51.7× | 0.026 | ADAM10 |
| Axon guidance | 1 | 45.1× | 0.029 | ADAM10 |
GO biological processes by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| GO term | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| constitutive protein ectodomain proteolysis | 1 | 16852.0× | 9e-04 | ADAM10 |
| regulation of vasculature development | 1 | 16852.0× | 9e-04 | ADAM10 |
| epidermal growth factor receptor ligand maturation | 1 | 8426.0× | 0.001 | ADAM10 |
| protein catabolic process at postsynapse | 1 | 5617.3× | 0.001 | ADAM10 |
| postsynapse organization | 1 | 2407.4× | 0.002 | ADAM10 |
| monocyte activation | 1 | 1872.4× | 0.002 | ADAM10 |
| pore complex assembly | 1 | 1872.4× | 0.002 | ADAM10 |
| amyloid precursor protein catabolic process | 1 | 1203.7× | 0.003 | ADAM10 |
| positive regulation of T cell chemotaxis | 1 | 1123.5× | 0.003 | ADAM10 |
| positive regulation of tumor necrosis factor-mediated signaling pathway | 1 | 1053.2× | 0.003 | ADAM10 |
| regulation of neurotransmitter receptor localization to postsynaptic specialization membrane | 1 | 887.0× | 0.003 | ADAM10 |
| regulation of Notch signaling pathway | 1 | 842.6× | 0.003 | ADAM10 |
| membrane protein ectodomain proteolysis | 1 | 648.1× | 0.003 | ADAM10 |
| response to tumor necrosis factor | 1 | 624.1× | 0.003 | ADAM10 |
| regulation of postsynapse organization | 1 | 526.6× | 0.004 | ADAM10 |
| adherens junction organization | 1 | 510.7× | 0.004 | ADAM10 |
| cochlea development | 1 | 468.1× | 0.004 | ADAM10 |
| negative regulation of cell adhesion | 1 | 383.0× | 0.004 | ADAM10 |
| extracellular matrix disassembly | 1 | 366.4× | 0.004 | ADAM10 |
| epidermal growth factor receptor signaling pathway | 1 | 247.8× | 0.006 | ADAM10 |
| positive regulation of cell growth | 1 | 183.2× | 0.008 | ADAM10 |
| protein processing | 1 | 170.2× | 0.008 | ADAM10 |
| integrin-mediated signaling pathway | 1 | 160.5× | 0.008 | ADAM10 |
| positive regulation of tumor necrosis factor production | 1 | 153.2× | 0.008 | ADAM10 |
| Notch signaling pathway | 1 | 141.6× | 0.008 | ADAM10 |
| in utero embryonic development | 1 | 72.0× | 0.016 | ADAM10 |
| cell-cell signaling | 1 | 69.6× | 0.016 | ADAM10 |
| negative regulation of gene expression | 1 | 69.1× | 0.016 | ADAM10 |
| positive regulation of cell migration | 1 | 61.7× | 0.017 | ADAM10 |
| positive regulation of cell population proliferation | 1 | 33.6× | 0.030 | ADAM10 |
Therapeutics
Drug target analysis
Approved (phase 4): 0 · Phase ≥3: 0 · Phased (≥1): 1 · Undrugged: 0
Druggability breadth: 1 of 1 evidence-associated genes (100%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).
Top cohort targets by molecule count
| Symbol | Molecules | Max phase |
|---|---|---|
| ADAM10 | 2 | 2 |
Drugs targeting cohort genes (top 30)
| Molecule | Max phase | Targets in cohort |
|---|---|---|
| ILOMASTAT | 2 | ADAM10 |
| APRATASTAT | 2 | ADAM10 |
Bioactivity and enzyme data
Enzyme cohort genes (≥1 EC): 1.
Cohort genes with ChEMBL bioactivity (full, sorted by assay count)
| Symbol | Assays | Type breakdown |
|---|---|---|
| ADAM10 | 64 | Binding:60, ADMET:4 |
Cohort enzymes (BRENDA EC)
| Symbol | EC numbers | Names |
|---|---|---|
| ADAM10 | 3.4.24.81 | ADAM10 endopeptidase |
Pharmacogenomics
Cohort genes with a PharmGKB record: 1; with CPIC/DPWG dosing guidelines: 0.
No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).
Chemical tractability of cohort targets
2 approved/phased compounds have measured bioactivity against a cohort gene (and aren’t yet in disease-level trials). This is a research / tractability signal, NOT a therapeutic recommendation — a bioactivity row often reflects off-target or screening binding (e.g. promiscuous kinase inhibitors against a cohort kinase), implying no disease mechanism.
| Compound | Max phase | Cohort target (bioactivity) |
|---|---|---|
| ILOMASTAT | 2 | ADAM10 |
| APRATASTAT | 2 | ADAM10 |
Druggability pyramid
Cohort genes binned by druggability tier (high → low):
| Tier | Definition | Genes | Symbols |
|---|---|---|---|
| A | Approved (phase 4 drug) | 0 | |
| B | Phased (≥1) drug, not yet approved | 1 | ADAM10 |
| C | Druggable family + PDB, no drug | 0 | |
| D | Druggable family + AlphaFold only, no drug | 0 | |
| E | Difficult family or no structure, no drug | 0 |
Undrugged target profiles
0 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).
Clinical trials & evidence
Clinical trials
Clinical trials: 2.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05637801 | Not specified | ACTIVE_NOT_RECRUITING | A Pivotal Study of Sensory Stimulation in Alzheimer’s Disease (HOPE Study) |
| NCT04100889 | Not specified | WITHDRAWN | A Non-Interventional Pilot Study to Explore the Role of Gut Flora in Alzheimer’s Disease |
Related Atlas pages
- Cohort genes: ADAM10