CausalSentinel

Protein Dossier — KLK13 (Kallikrein-13)

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
Years of schooling 0.0309 0.0103 0.0027 Wald ratio 1 cis NA
Serum cystatin C (eGFRcys) 0.0149 0.00567 0.00838 Wald ratio 1 cis NA
Alzheimer’s disease -0.112 0.0438 0.0107 Wald ratio 1 cis NA
Diagnoses - main ICD10: R07 Pain in throat and chest -0.0743 0.0312 0.0171 Wald ratio 1 cis NA
Diagnoses - main ICD10: I83 Varicose veins of lower extremities 0.0959 0.0412 0.0199 Wald ratio 1 cis NA
Diagnoses - main ICD10: H25 Senile cataract 0.137 0.0647 0.0346 Wald ratio 1 cis NA
Neo-agreeableness -0.356 0.176 0.0424 Wald ratio 1 cis NA
Lung adenocarcinoma -0.149 0.0774 0.0542 Wald ratio 1 cis NA
Diagnoses - main ICD10: N81 Female genital prolapse 0.0944 0.0494 0.056 Wald ratio 1 cis NA
Coronary heart disease 0.0481 0.0263 0.0667 Wald ratio 1 cis NA
Non-cancer illness code self-reported: bladder problem (not cancer) -0.184 0.103 0.0753 Wald ratio 1 cis NA
Non-cancer illness code self-reported: pernicious anaemia 0.178 0.101 0.0786 Wald ratio 1 cis NA
…and 74 more outcomes (see JSON)              

2. pQTL instrument availability (Tier-B probe)

Dataset Trait Author Year
prot-c-3200_49_2 kallikrein 13 Suhre K 2019

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

60 association rows across 23 traits (60 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 KLK12 levels 6e-2130 rs62117666 5 GCST90860580 no MR -> candidate analysis
Circulating KLK13 levels 3e-1112 rs3760739 4 GCST90860002 no MR -> candidate analysis
Kallikrein-13 levels 3e-189 rs2569459 5 GCST90248158 no MR -> candidate analysis
KLK12 protein levels 2e-182 rs77342236 11 GCST90469698 no MR -> candidate analysis
KLK13 protein levels 2e-110 rs7253072 5 GCST90469699 no MR -> candidate analysis
Circulating KLK10 levels 8e-101 rs3760744 1 GCST90860356 no MR -> candidate analysis
KLK14 protein levels 2e-96 rs2569459 4 GCST90469700 no MR -> candidate analysis
Serum levels of protein KLK13 1e-79 rs2569459 3 GCST90086572 no MR -> candidate analysis
Blood protein levels 4e-54 rs3760739 2 GCST006585 no MR -> candidate analysis
Kallikrein-12 levels 5e-50 rs8103941 3 GCST90101221 no MR -> candidate analysis
Kallikrein-13 (analyte X11152.46) levels 2e-48 rs34089525 1 GCST90421334 no MR -> candidate analysis
Circulating KLK14 levels 1e-44 rs8103083 1 GCST90860034 no MR -> candidate analysis
…and 11 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 309 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
actinic keratosis 0.275 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 (Kallikrein-13)
gnomAD constraint pLI=2.2e-06, LOEUF=1.24 — LoF-tolerant
GWAS Catalog 199 unique SNPs / 474 rows
ClinVar 76 records; 0 pathogenic in sample of 30
PharmGKB/ClinPGx no annotations

Caveats declared by the tools

Sources

Provenance