CausalSentinel

Protein Dossier — IL1R2 (Interleukin-1 receptor type 2)

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
Ulcerative colitis 0.196 0.0319 7.61e-10 Wald ratio 1 cis 0.00971
Inflammatory bowel disease 0.153 0.0252 1.37e-09 Wald ratio 1 cis 2.46e-09
Non-cancer illness code self-reported: asthma -0.0756 0.0185 4.20e-05 Wald ratio 1 cis NA
Crohn’s disease 0.12 0.0306 8.61e-05 Wald ratio 1 cis NA
Forced vital capacity (FVC) -0.0171 0.00501 6.31e-04 Wald ratio 1 cis NA
Diagnoses - main ICD10: G56 Mononeuropathies of upper limb 0.137 0.0405 6.97e-04 Wald ratio 1 cis NA
Body mass index (BMI) 0.0196 0.0061 0.00131 Wald ratio 1 cis NA
PGC cross-disorder traits 0.0879 0.0303 0.00374 Wald ratio 1 cis NA
Diagnoses - main ICD10: G47 Sleep disorders 0.188 0.0663 0.00464 Wald ratio 1 cis NA
Non-cancer illness code self-reported: hypertension 0.0281 0.0101 0.00542 Wald ratio 1 cis NA
Femoral neck bone mineral density -0.0524 0.019 0.00576 Wald ratio 1 cis NA
Depressive symptoms 0.0199 0.00745 0.00766 Wald ratio 1 cis NA
…and 111 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

53 association rows across 30 traits (44 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
Circulating IL1R2 levels 1e-2261 rs2310170 3 GCST90859972 no MR -> candidate analysis
Interleukin-1 receptor type 2 levels 5e-255 rs2310170 6 GCST90248054 no MR -> candidate analysis
IL1R2 protein levels 3e-220 rs554778901 10 GCST90469572 no MR -> candidate analysis
Circulating IL1R1 levels 2e-144 rs10185424 2 GCST90859959 no MR -> candidate analysis
IL1R1 protein levels 3e-111 rs4851533 1 GCST90469571 no MR -> candidate analysis
Serum levels of protein IL1R2 1e-104 rs7561191 1 GCST90087809 no MR -> candidate analysis
Interleukin-1 receptor type 1 levels 9e-64 rs7587167 1 GCST90425563 no MR -> candidate analysis
Interleukin-1 receptor type 2 levels (IL1R2.14133.93.3) 6e-62 rs7561460 1 GCST90241579 no MR -> candidate analysis
Blood protein levels 7e-55 rs7561460 1 GCST006585 no MR -> candidate analysis
IL1RL2 protein levels 2e-45 rs719250 2 GCST90469575 no MR -> candidate analysis
IL1RL1 protein levels 8e-44 rs4141134 2 GCST90469574 no MR -> candidate analysis
Cerebrospinal fluid protein IL1R1 levels 5e-42 rs11685537 1 GCST90944793 no MR -> candidate analysis
…and 18 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 457 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
inflammatory bowel disease 0.641 common-variant locus MR: beta=0.153, p=1.37e-09 (cis)
asthma 0.608 common-variant locus MR: beta=-0.0756, p=4.20e-05 (cis)
pneumonia 0.507 common-variant locus no MR -> candidate analysis
ulcerative colitis 0.444 common-variant locus MR: beta=0.196, p=7.61e-10 (cis)
infectious meningitis 0.417 common-variant locus no MR -> candidate analysis
chronic rhinosinusitis 0.272 common-variant locus no MR -> candidate analysis
Meniere disease 0.2 common-variant locus no MR -> candidate analysis
gout 0.215 common-variant locus MR: beta=0.049, p=0.316 (cis)
body weight gain 0.202 common-variant locus no MR -> candidate analysis
eye disorder 0.174 common-variant locus no MR -> candidate analysis
coronary artery disorder 0.068 common-variant locus no MR -> candidate analysis
Parkinson disease 0.044 common-variant locus no MR -> candidate analysis

Of the 12 rows above, 8 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=2.5e-18, LOEUF=1.49 — LoF-tolerant
GWAS Catalog 119 unique SNPs / 208 rows
ClinVar 106 records; 0 pathogenic in sample of 30
PharmGKB/ClinPGx no annotations

Caveats declared by the tools

Sources

Provenance