CausalSentinel

Protein Dossier — LGALS3BP (Galectin-3-binding protein)

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
PGC cross-disorder traits -0.225 0.0888 0.0114 Wald ratio 1 cis NA
Non-cancer illness code self-reported: psoriasis 0.288 0.116 0.0134 Wald ratio 1 cis NA
Non-cancer illness code self-reported: asthma -0.122 0.0515 0.0179 Wald ratio 1 cis NA
Autism -0.435 0.199 0.0288 Wald ratio 1 cis NA
Diagnoses - main ICD10: R35 Polyuria 0.387 0.184 0.0356 Wald ratio 1 cis NA
Forced vital capacity (FVC) -0.0275 0.0133 0.0387 Wald ratio 1 cis NA
Major depressive disorder -0.317 0.156 0.042 Wald ratio 1 cis NA
Diagnoses - main ICD10: L03 Cellulitis 0.274 0.141 0.0516 Wald ratio 1 cis NA
Fractured bone site(s): Ankle 0.215 0.113 0.0577 Wald ratio 1 cis NA
Sleep duration 0.0233 0.0127 0.0662 Wald ratio 1 cis NA
Cancer code self-reported: prostate cancer 0.264 0.15 0.0789 Wald ratio 1 cis NA
Vascular or heart problems diagnosed by doctor: Angina 0.139 0.0798 0.0818 Wald ratio 1 cis NA
…and 71 more outcomes (see JSON)              

2. pQTL instrument availability (Tier-B probe)

Dataset Trait Author Year
prot-c-5000_52_1 LG3BP Suhre K 2019

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

26 association rows across 15 traits (23 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
LGALS3BP protein levels 1e-77 rs111526614 3 GCST90469760 no MR -> candidate analysis
CANT1 protein levels 1e-58 rs112832453 1 GCST90468536 no MR -> candidate analysis
Galectin-3-binding protein levels 4e-35 rs111526614 5 GCST90247672 no MR -> candidate analysis
Circulating DSG4 levels 3e-30 rs55842605 1 GCST90860253 no MR -> candidate analysis
DSG4 protein levels 3e-29 rs55842605 1 GCST90469044 no MR -> candidate analysis
DSG3/DSG4 protein level ratio 2e-27 rs7220336 1 GCST90314558 no MR -> candidate analysis
Height 7e-17 rs4789915 3 GCST90245848 no MR -> candidate analysis
Serum levels of protein LGALS3BP 2e-12 rs3826311 1 GCST90088859 no MR -> candidate analysis
Total PHF-tau (SNP x SNP interaction) 2e-12 rs4789907 x rs1124952 3 GCST010340 no MR -> candidate analysis
Physical function (baseline) 2e-10 rs56352914 1 GCST90565837 no MR -> candidate analysis
Metalloproteinase inhibitor 2 levels 4e-10 rs4789927 1 GCST90424491 no MR -> candidate analysis
Protein quantitative trait loci (liver) 2e-8 rs58996443 1 GCST011427 no MR -> candidate analysis
…and 3 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 339 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
metabolic disease 0.457 common-variant locus no MR -> candidate analysis

Of the 1 rows above, 1 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 0 known modulators (Galectin-3-binding protein)
gnomAD constraint pLI=7.6e-10, LOEUF=1.53 — LoF-tolerant
GWAS Catalog 65 unique SNPs / 130 rows
ClinVar 131 records; 1 pathogenic in sample of 30
PharmGKB/ClinPGx no annotations

Caveats declared by the tools

Sources

Provenance