CausalSentinel

Protein Dossier — LRP11 (Low-density lipoprotein receptor-related protein 11)

MR feasibility tier: A — Published pQTL-MR estimates exist for this protein (retrieved below - not computed here).

1. Published MR estimates (retrieved, not computed)

Outcome beta se p method nSNP cis/trans coloc
Internalizing problems 0.087 0.0275 0.00156 Wald ratio 1 cis NA
Pallidum volume 7.21 2.34 0.00209 Wald ratio 1 cis NA
Potassium in urine 0.00832 0.00303 0.00596 Wald ratio 1 cis NA
Hearing difficulty or problems: Yes 0.0131 0.00508 0.0102 Wald ratio 1 cis NA
Mean cell haemoglobin concentration -0.0112 0.00436 0.0106 Wald ratio 1 cis NA
Age at menarche -0.0206 0.00839 0.014 Wald ratio 1 cis NA
Non-cancer illness code self-reported: hypertension -0.0118 0.00515 0.0215 Wald ratio 1 cis NA
Heel bone mineral density (BMD) T-score automated 0.00875 0.00386 0.0234 Wald ratio 1 cis NA
Serum creatinine (eGFRcrea) 0.00242 0.00112 0.0297 Wald ratio 1 cis NA
Cancer code self-reported: malignant melanoma -0.0796 0.0367 0.03 Wald ratio 1 cis NA
Parkinson’s disease -0.109 0.0502 0.0302 Wald ratio 1 cis NA
Urate 0.0158 0.00727 0.0303 Wald ratio 1 cis NA
…and 106 more outcomes (see JSON)              

2. pQTL instrument availability (Tier-B probe)

No prot-* pQTL GWAS dataset found for this protein (matched by UniProt accession and symbol).

3. GWAS Catalog results — traits with signal at this locus

33 association rows across 29 traits (31 genome-wide significant rows). Associations are loci, not causal claims; the mapped gene at a locus is not necessarily the effector gene.

Trait best p lead SNP n assoc study MR status
Low-density lipoprotein receptor-related protein 11 levels 2e-1411 rs9322225 1 GCST90248262 no MR -> candidate analysis
Circulating LRP11 levels 4e-79 rs142987810 1 GCST90860386 no MR -> candidate analysis
LRP11 protein levels 4e-58 rs142987810 4 GCST90469796 no MR -> candidate analysis
Brain morphology (MOSTest) 2e-31 rs7752089 1 GCST90239729 no MR -> candidate analysis
Low-density lipoprotein receptor-related protein 11 (analyte 4e-23 rs1889471 1 GCST90422684 no MR -> candidate analysis
Macular thickness 3e-19 rs14314 1 GCST006976 no MR -> candidate analysis
5-methylthioadenosine (mta) levels 3e-18 rs869109015 1 GCST90139562 no MR -> candidate analysis
Vertex-wise sulcal depth 7e-17 rs14314 1 GCST90095129 no MR -> candidate analysis
Cerebrospinal fluid 5-methylthioadenosine (MTA) levels 4e-16 rs1889473 1 GCST90318216 no MR -> candidate analysis
Plasma S-adenosylhomocysteine (SAH) levels in chronic kidney 4e-16 rs14314 1 GCST90265918 no MR -> candidate analysis
Inosine triphosphate pyrophosphatase protein levels (SomaSca 2e-15 rs1889473 1 GCST90438881 no MR -> candidate analysis
Left hippocampal volume (body) 7e-15 rs14314 1 GCST90267904 no MR -> candidate analysis
…and 17 more traits (see JSON)          

4. Phenome map — where this gene is a genetic locus, vs. where MR exists

Top diseases by Open Targets association (of 129 total). Associations are loci, not causal claims. The causal-status column is a four-state triage per pair: established (curated) = a curated clinical assertion exists (ClinGen/G2P/GEL/Orphanet/ClinVar — any validity level, MR adds little); exploratory rare-variant signal = ExWAS burden evidence without curation — a candidate NEW gene-disease relationship; common-variant locus = GWAS signal, classic pQTL-MR territory; multi-layer = burden+GWAS together, an allelic-series candidate (the strongest causal setup). Burden estimand is carrier-vs-noncarrier, not per-SD MR.

Disease genetic assoc. burden (ExWAS) causal status MR status
mixed connective tissue disease 0.391 common-variant locus no MR -> candidate analysis
testicular germ cell tumor 0.198 common-variant locus no MR -> candidate analysis
migraine disorder 0.16 common-variant locus no MR -> candidate analysis
binge eating disorder 0.15 common-variant locus no MR -> candidate analysis
hypertrophic cardiomyopathy 0.151 common-variant locus no MR -> candidate analysis

Of the 5 rows above, 5 have no MR estimate in this resource. Across all retrieved diseases for this gene: 0 exploratory rare-variant signal(s), 0 multi-layer (allelic-series candidate) pair(s). Final triage still belongs to a statistical geneticist.

5. Downstream annotation (druggability & safety preview)

Layer Result
ChEMBL druggability not available — no ChEMBL target (undrugged)
gnomAD constraint pLI=5.3e-05, LOEUF=0.811 — LoF-tolerant
GWAS Catalog 86 unique SNPs / 172 rows
ClinVar 93 records; 2 pathogenic in sample of 30
PharmGKB/ClinPGx no annotations

Caveats declared by the tools

Sources

Provenance