CausalSentinel

Protein Dossier — KLK11 (Kallikrein-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
Sodium in urine -0.0101 0.00364 0.00554 Wald ratio 1 cis NA
Non-cancer illness code self-reported: high cholesterol -0.0252 0.0103 0.014 Wald ratio 1 cis NA
Eye problems or disorders: Diabetes related eye disease 0.0979 0.043 0.0229 Wald ratio 1 cis NA
Diagnoses - main ICD10: G47 Sleep disorders -0.124 0.0549 0.0233 Wald ratio 1 cis NA
Non-cancer illness code self-reported: uterine fibroids -0.0729 0.0322 0.0235 Wald ratio 1 cis NA
Microalbuminuria -0.0918 0.0434 0.0344 Wald ratio 1 cis NA
Urinary albumin-to-creatinine ratio -0.0309 0.015 0.0398 Wald ratio 1 cis NA
Non-cancer illness code self-reported: gout -0.0671 0.0332 0.0434 Wald ratio 1 cis NA
Serum cystatin C (eGFRcys) 0.0076 0.00384 0.0479 Wald ratio 1 cis NA
Creatinine (enzymatic) in urine -0.00689 0.00354 0.0521 Wald ratio 1 cis NA
Potassium in urine -0.00704 0.00376 0.0612 Wald ratio 1 cis NA
Rheumatoid arthritis -0.0486 0.026 0.0616 Wald ratio 1 cis NA
…and 89 more outcomes (see JSON)              

2. pQTL instrument availability (Tier-B probe)

Dataset Trait Author Year
prot-c-2831_29_1 Kallikrein 11 Suhre K 2019

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

33 association rows across 22 traits (32 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
kallikrein-11 levels 2e-1041 rs1048328 9 GCST90248156 no MR -> candidate analysis
Circulating KLK10 levels 1e-777 rs2691208 1 GCST90860356 no MR -> candidate analysis
Kallikrein-11 (analyte X2831.29) levels 1e-394 rs1048328 1 GCST90425490 no MR -> candidate analysis
Kallikrein-11 (analyte X7775.15) levels 5e-379 rs1048328 1 GCST90427060 no MR -> candidate analysis
Blood protein levels 1e-261 rs1048328 2 GCST006585 no MR -> candidate analysis
Circulating KLK11 levels 5e-186 rs62117662 1 GCST90860017 no MR -> candidate analysis
Kallikrein-11 levels (KLK11.2831.29.1) 6e-186 rs1048328 1 GCST90241670 no MR -> candidate analysis
KLK11 protein levels 2e-178 rs62117662 2 GCST90469697 no MR -> candidate analysis
Serum levels of protein KLK11 6e-153 rs1048328 1 GCST90089823 no MR -> candidate analysis
Protein S100-P levels 7e-56 rs1048328 1 GCST90427997 no MR -> candidate analysis
Kallikrein-10 levels 2e-33 rs3745539 1 GCST90179343 no MR -> candidate analysis
KLK7 protein levels 9e-29 rs143406762 1 GCST90469706 no MR -> candidate analysis
…and 10 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 412 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
ichthyosis with erythrokeratoderma 0.745 established (curated) no MR -> candidate analysis
hereditary disease 0.315 established (curated) no MR -> candidate analysis

Of the 2 rows above, 2 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 (Kallikrein-11)
gnomAD constraint pLI=0.22, LOEUF=0.725 — LoF-tolerant
GWAS Catalog 172 unique SNPs / 454 rows
ClinVar 78 records; 0 pathogenic in sample of 30
PharmGKB/ClinPGx no annotations

Caveats declared by the tools

Sources

Provenance