CausalSentinel

Protein Dossier — LANCL1 (Glutathione S-transferase LANCL1)

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
Cancer code self-reported: prostate cancer 0.471 0.149 0.00156 Wald ratio 1 cis NA
Diagnoses - main ICD10: G47 Sleep disorders 0.469 0.167 0.005 Wald ratio 1 cis NA
Eye problems or disorders: Injury or trauma resulting in loss of vision 0.435 0.175 0.0131 Wald ratio 1 cis NA
Diagnoses - main ICD10: K29 Gastritis and duodenitis 0.226 0.104 0.0295 Wald ratio 1 cis NA
Eye problems or disorders: Cataract 0.188 0.0917 0.0408 Wald ratio 1 cis NA
Non-cancer illness code self-reported: asthma 0.1 0.0504 0.0473 Wald ratio 1 cis NA
Non-cancer illness code self-reported: kidney stone or ureter stone or bladder stone 0.327 0.167 0.0498 Wald ratio 1 cis NA
Potassium in urine 0.0386 0.0201 0.0554 Wald ratio 1 cis NA
ER-negative Breast cancer (Combined Oncoarray; iCOGS; GWAS meta analysis) -0.204 0.107 0.056 Wald ratio 1 cis NA
Diagnoses - main ICD10: H25 Senile cataract 0.323 0.169 0.0566 Wald ratio 1 cis NA
Diagnoses - main ICD10: I83 Varicose veins of lower extremities -0.412 0.222 0.063 Wald ratio 1 cis NA
Forced vital capacity (FVC) -0.0297 0.0162 0.0672 Wald ratio 1 cis NA
…and 43 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

23 association rows across 19 traits (20 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
Glycine levels 4e-35 rs62202072 4 GCST90503747 no MR -> candidate analysis
Creatinine levels 1e-12 rs79675564 1 GCST90019502 no MR -> candidate analysis
Estimated glomerular filtration rate 2e-12 rs79675564 1 GCST90019506 no MR -> candidate analysis
Contracture of joint (PheCode 739) 8e-12 rs572240213 1 GCST90480542 no MR -> candidate analysis
CRYGD protein levels 1e-11 rs185471906 1 GCST90468876 no MR -> candidate analysis
Citrulline levels 1e-10 rs3732055 1 GCST90200403 no MR -> candidate analysis
Gamma-glutamylcitrulline levels 1e-10 rs3732055 1 GCST90200185 no MR -> candidate analysis
Age when finished full-time education (standard GWA) 7e-10 rs1585241 1 GCST90267280 no MR -> candidate analysis
Adult body size 3e-9 rs79675564 1 GCST010988 no MR -> candidate analysis
Educational attainment 4e-9 rs3900166 2 GCST90105038 no MR -> candidate analysis
Phospholipid levels in HDL 8e-9 rs754778318 1 GCST90092827 no MR -> candidate analysis
Total lipid levels in HDL 9e-9 rs754778318 1 GCST90092825 no MR -> candidate analysis
…and 7 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 168 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
Abnormality of the skeletal system 0.513 common-variant locus no MR -> candidate analysis
Pain 0.436 common-variant locus MR: beta=0.0769, p=0.352 (cis)
contracture 0.425 common-variant locus no MR -> candidate analysis
placental abruption 0.425 common-variant locus no MR -> candidate analysis
squamous cell carcinoma 0.11 common-variant locus no MR -> candidate analysis
adverse effect 0.11 common-variant locus no MR -> candidate analysis
response to stimulus 0.11 common-variant locus no MR -> candidate analysis

Of the 7 rows above, 6 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 (Glutathione S-transferase LANCL1)
gnomAD constraint pLI=2.5e-17, LOEUF=1.25 — LoF-tolerant
GWAS Catalog 57 unique SNPs / 114 rows
ClinVar 109 records; 1 pathogenic in sample of 30
PharmGKB/ClinPGx no annotations

Caveats declared by the tools

Sources

Provenance