CausalSentinel

Protein Dossier — ACP6 (Lysophosphatidic acid phosphatase type 6)

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 0.0143 0.00468 0.0022 Wald ratio 1 cis NA
Internalizing problems 0.0773 0.026 0.00289 Wald ratio 1 cis NA
Forced vital capacity (FVC) 0.00659 0.00229 0.00397 Wald ratio 1 cis NA
Diagnoses - main ICD10: H25 Senile cataract 0.0841 0.0292 0.00401 Wald ratio 1 cis NA
Body mass index (BMI) -0.00748 0.00279 0.00723 Wald ratio 1 cis NA
Forced expiratory volume in 1-second (FEV1) 0.00642 0.00241 0.00782 Wald ratio 1 cis NA
Bulimia nervosa 0.0222 0.00847 0.00866 Wald ratio 1 cis NA
Systolic blood pressure automated reading -0.00748 0.00285 0.00869 Wald ratio 1 cis NA
Diagnoses - main ICD10: I30 Acute pericarditis 0.308 0.119 0.00932 Wald ratio 1 cis NA
Diagnoses - main ICD10: D25 Leiomyoma of uterus 0.0589 0.0232 0.0111 Wald ratio 1 cis NA
Diagnoses - main ICD10: I48 Atrial fibrillation and flutter 0.0613 0.0248 0.0135 Wald ratio 1 cis NA
Alcohol intake frequency -0.0101 0.00412 0.014 Wald ratio 1 cis NA
…and 93 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

41 association rows across 18 traits (39 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 ACP6 levels 2e-4526 rs28700004 3 GCST90860337 no MR -> candidate analysis
Lysophosphatidic acid phosphatase type 6 levels 7e-1466 rs2153463 6 GCST90248244 no MR -> candidate analysis
Cerebrospinal fluid protein ACP6 levels 4e-407 rs2153463 1 GCST90942987 no MR -> candidate analysis
Blood protein levels 2e-312 rs2153463 1 GCST006585 no MR -> candidate analysis
ACP6 protein levels 2e-219 rs150066520 13 GCST90468204 no MR -> candidate analysis
Serum levels of protein ACP6 7e-171 rs75583687 2 GCST90089187 no MR -> candidate analysis
Lysophosphatidic acid phosphatase type 6 level in Chronic ki 6e-78 rs2153463 1 GCST90238074 no MR -> candidate analysis
Height 2e-72 rs12129752 1 GCST90245848 MR: beta=0.00773, p=0.0225 (cis)
X-24747 levels 2e-63 rs6674938 1 GCST90103336 no MR -> candidate analysis
X-24309 levels 2e-41 rs2153463 2 GCST90245747 no MR -> candidate analysis
Hemopexin protein levels (SomaScan ID:5742-14) 3e-20 rs1344 1 GCST90438035 no MR -> candidate analysis
Cerebrospinal fluid metabolite X-12411 levels 2e-15 rs2275552 1 GCST90318302 no MR -> candidate analysis
…and 6 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 59 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
ventricular septal defect 0.538 common-variant locus no MR -> candidate analysis
dermatophytosis 0.502 common-variant locus no MR -> candidate analysis
Rare genetic intellectual disability with developmental anomaly 0.438 established (curated) no MR -> candidate analysis
gallbladder disorder 0.393 common-variant locus no MR -> candidate analysis
response to anticoagulant 0.309 common-variant locus no MR -> candidate analysis

Of the 5 rows above, 5 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 not available — no ChEMBL target (undrugged)
gnomAD constraint pLI=8.3e-17, LOEUF=1.27 — LoF-tolerant
GWAS Catalog 88 unique SNPs / 176 rows
ClinVar 393 records; 12 pathogenic in sample of 30
PharmGKB/ClinPGx no annotations

Caveats declared by the tools

Sources

Provenance