CausalSentinel

Protein Dossier — DAPK2 (Death-associated protein kinase 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
Diagnoses - main ICD10: I30 Acute pericarditis 0.592 0.213 0.0055 Wald ratio 1 cis NA
Non-cancer illness code self-reported: chronic obstructive airways disease or copd 0.235 0.0874 0.00714 Wald ratio 1 cis NA
Creatinine (enzymatic) in urine 0.016 0.00613 0.00922 Wald ratio 1 cis NA
Packed cell volume -0.124 0.0486 0.0105 Wald ratio 1 cis NA
Non-cancer illness code self-reported: psoriasis 0.131 0.053 0.0132 Wald ratio 1 cis NA
Diagnoses - main ICD10: N92 Excessive frequent and irregular menstruation 0.0994 0.0404 0.0139 Wald ratio 1 cis NA
LDL cholesterol 0.0337 0.0138 0.0146 Wald ratio 1 cis NA
Chronic kidney disease -0.0955 0.0398 0.0164 Wald ratio 1 cis NA
HDL cholesterol 0.0303 0.0127 0.0175 Wald ratio 1 cis NA
Diagnoses - main ICD10: G47 Sleep disorders 0.165 0.0711 0.02 Wald ratio 1 cis NA
Diagnoses - main ICD10: K43 Ventral hernia 0.184 0.0805 0.0223 Wald ratio 1 cis NA
Diagnoses - main ICD10: R10 Abdominal and pelvic pain -0.0736 0.0333 0.0271 Wald ratio 1 cis NA
…and 98 more outcomes (see JSON)              

2. pQTL instrument availability (Tier-B probe)

Dataset Trait Author Year
prot-c-4355_13_1 DAPK2 Suhre K 2019

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

43 association rows across 32 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
Death-associated protein kinase 2 levels 2e-150 rs4436737 3 GCST90247234 no MR -> candidate analysis
Death-associated protein kinase 1 levels 2e-117 rs55986634 1 GCST90247233 no MR -> candidate analysis
DAPK2 protein levels 5e-109 rs2414840 7 GCST90468945 no MR -> candidate analysis
Hematological traits (multi-trait analysis) 3e-18 rs187236774 1 GCST90838669 no MR -> candidate analysis
Height 3e-15 rs17788704 3 GCST90245848 MR: beta=0.00557, p=0.469 (cis)
HDL cholesterol levels 4e-15 rs34675318 1 GCST010242 no MR -> candidate analysis
Thyroid stimulating hormone levels 2e-14 rs1542244 1 GCST90572789 no MR -> candidate analysis
Standing height (UKB data field 50) 3e-12 rs145586222 1 GCST90468178 no MR -> candidate analysis
Mean corpuscular volume 7e-12 rs72755040 1 GCST90056174 no MR -> candidate analysis
Height (baseline) 3e-11 rs17775820 1 GCST90565843 no MR -> candidate analysis
Platelet distribution width 6e-10 rs141207816 1 GCST004616 no MR -> candidate analysis
Gut microbial network clusters (Salmon (at 1 year) x Any Bre 3e-9 rs72755006 1 GCST90569450 no MR -> candidate analysis
…and 20 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 124 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
alcohol drinking 0.536 common-variant locus no MR -> candidate analysis
eye disorder 0.394 common-variant locus no MR -> candidate analysis
hypothyroidism 0.106 common-variant locus no MR -> candidate analysis
placental abruption 0.049 common-variant locus no MR -> candidate analysis
gastric ulcer 0.045 common-variant locus no MR -> candidate analysis
hemorrhage 0.045 common-variant locus no MR -> candidate analysis
IgA glomerulonephritis 0.04 common-variant locus no MR -> candidate analysis

Of the 7 rows above, 7 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 (Death-associated protein kinase 2)
gnomAD constraint pLI=3.8e-10, LOEUF=1.05 — LoF-tolerant
GWAS Catalog 75 unique SNPs / 146 rows
ClinVar 99 records; 0 pathogenic in sample of 30
PharmGKB/ClinPGx no annotations

Caveats declared by the tools

Sources

Provenance