CausalSentinel

Protein Dossier — GSTP1 (Glutathione S-transferase P)

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
Weight 0.0535 0.0125 1.79e-05 Wald ratio 1 cis NA
Mean cell volume 0.612 0.153 6.14e-05 Wald ratio 1 cis NA
Mean cell haemoglobin 0.217 0.0601 2.98e-04 Wald ratio 1 cis NA
Diagnoses - main ICD10: K29 Gastritis and duodenitis 0.245 0.072 6.45e-04 Wald ratio 1 cis NA
Endometrioid ovarian cancer -0.449 0.169 0.00795 Wald ratio 1 cis NA
Knee osteoarthritis 0.407 0.154 0.00822 Wald ratio 1 cis NA
Sleep duration -0.0252 0.011 0.0222 Wald ratio 1 cis NA
Diagnoses - main ICD10: M17 Gonarthrosis [arthrosis of knee] 0.193 0.0846 0.0222 Wald ratio 1 cis NA
Red blood cell count -0.0281 0.0129 0.0297 Wald ratio 1 cis NA
Non-cancer illness code self-reported: depression 0.113 0.0522 0.0305 Wald ratio 1 cis NA
Non-cancer illness code self-reported: asthma 0.0773 0.0367 0.0351 Wald ratio 1 cis NA
Percent emphysema -0.222 0.111 0.045 Wald ratio 1 cis NA
…and 104 more outcomes (see JSON)              

2. pQTL instrument availability (Tier-B probe)

Dataset Trait Author Year
prot-c-4911_49_2 Glutathione S-transferase Pi Suhre K 2019

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

30 association rows across 26 traits (29 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
Glutathione S-transferase P (analyte X4911.49) levels 5e-315 rs1695 1 GCST90426141 no MR -> candidate analysis
Circulating GSTP1 levels 1e-217 rs7927657 2 GCST90860696 no MR -> candidate analysis
GSTP1 protein levels 1e-210 rs762803 2 GCST90469414 no MR -> candidate analysis
Hematological traits (multi-trait analysis) 3e-192 rs6591250 1 GCST90838669 no MR -> candidate analysis
Height (baseline) 7e-43 rs145044531 1 GCST90565843 no MR -> candidate analysis
Glutathione S-transferase P levels 4e-39 rs11227841 1 GCST90247750 no MR -> candidate analysis
N-acetylglycine levels 4e-29 rs640777 3 GCST90245320 no MR -> candidate analysis
Cis-3,4-methyleneheptanoylglycine levels 4e-20 rs596603 1 GCST90200274 no MR -> candidate analysis
Hip circumference adjusted for BMI 7e-17 rs36051467 1 GCST012227 no MR -> candidate analysis
2-butenoylglycine levels 3e-16 rs596603 1 GCST90200152 no MR -> candidate analysis
Glutathione S-transferase P level in Chronic kidney disease 8e-15 rs1695 1 GCST90237743 no MR -> candidate analysis
Metabolite levels (N-acetyltryptophan) 2e-14 rs35297589 1 GCST90300142 no MR -> candidate analysis
…and 14 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 760 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
connective tissue neoplasm 0.21 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 1 known modulators (Glutathione S-transferase P)
gnomAD constraint pLI=8.2e-10, LOEUF=1.3 — LoF-tolerant
GWAS Catalog 72 unique SNPs / 144 rows
ClinVar 83 records; 1 pathogenic in sample of 30
PharmGKB/ClinPGx 22 clinical annotations across 17 drugs

Caveats declared by the tools

Sources

Provenance