CausalSentinel

Protein Dossier — DPP7 (Dipeptidyl peptidase 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
Non-cancer illness code self-reported: hypertension -0.0433 0.0135 0.00132 Wald ratio 1 cis NA
Diagnoses - main ICD10: R10 Abdominal and pelvic pain -0.107 0.0408 0.00891 Wald ratio 1 cis NA
Clear cell ovarian cancer 0.305 0.137 0.0261 Wald ratio 1 cis NA
Diagnoses - main ICD10: J33 Nasal polyp 0.194 0.0915 0.0339 Wald ratio 1 cis NA
Non-cancer illness code self-reported: arthritis (nos) 0.156 0.0751 0.0376 Wald ratio 1 cis NA
Hirschsprung’s disease -0.962 0.473 0.042 Wald ratio 1 cis NA
Eczema -0.125 0.0623 0.0444 Wald ratio 1 cis NA
Diagnoses - main ICD10: K80 Cholelithiasis -0.119 0.0597 0.0461 Wald ratio 1 cis NA
Non-cancer illness code self-reported: psoriasis -0.163 0.0847 0.0542 Wald ratio 1 cis NA
Birth weight -0.0228 0.0121 0.0592 Wald ratio 1 cis NA
Non-cancer illness code self-reported: vaginal prolapse or uterine prolapse 0.165 0.0879 0.0606 Wald ratio 1 cis NA
Non-cancer illness code self-reported: asthma -0.0401 0.0221 0.0699 Wald ratio 1 cis NA
…and 57 more outcomes (see JSON)              

2. pQTL instrument availability (Tier-B probe)

Dataset Trait Author Year
prot-c-3608_12_1 DPP2 Suhre K 2019

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

23 association rows across 19 traits (23 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
DPP7/SIAE protein level ratio 1e-1546 rs10747049 1 GCST90314549 no MR -> candidate analysis
DPP7/TPP1 protein level ratio 7e-1468 rs10747049 1 GCST90314550 no MR -> candidate analysis
DPP7/MCFD2 protein level ratio 3e-1460 rs10747049 1 GCST90314547 no MR -> candidate analysis
DPP7/GLB1 protein level ratio 9e-1338 rs10747049 1 GCST90314545 no MR -> candidate analysis
ARSA/DPP7 protein level ratio 3e-1288 rs10747049 1 GCST90313353 no MR -> candidate analysis
ARSB/DPP7 protein level ratio 3e-1277 rs10747049 1 GCST90313358 no MR -> candidate analysis
CREG1/DPP7 protein level ratio 6e-1263 rs10747049 1 GCST90314248 no MR -> candidate analysis
DPP7/PLA2G15 protein level ratio 1e-1249 rs10747049 1 GCST90314548 no MR -> candidate analysis
CANT1/DPP7 protein level ratio 3e-1168 rs10747049 1 GCST90313614 no MR -> candidate analysis
DPP7/LGMN protein level ratio 7e-1110 rs10747049 1 GCST90314546 no MR -> candidate analysis
DPP7/VSIR protein level ratio 2e-1071 rs10747049 1 GCST90314551 no MR -> candidate analysis
Dipeptidyl peptidase 2 levels 3e-513 rs10747049 5 GCST90247349 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 115 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 0.067 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 (Dipeptidyl peptidase 2)
gnomAD constraint pLI=8.5e-31, LOEUF=1.53 — LoF-tolerant
GWAS Catalog 71 unique SNPs / 142 rows
ClinVar 278 records; 1 pathogenic in sample of 30
PharmGKB/ClinPGx no annotations

Caveats declared by the tools

Sources

Provenance