CausalSentinel

Protein Dossier — CAPG (Condensin complex subunit 3)

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
Hearing difficulty or problems: Yes -0.0544 0.0141 1.18e-04 Wald ratio 1 cis NA
Forced vital capacity (FVC) -0.0184 0.00636 0.00376 Wald ratio 1 cis NA
Pulse rate 0.0381 0.0137 0.00542 Wald ratio 1 cis NA
Body mass index (BMI) 0.0215 0.00776 0.00558 Wald ratio 1 cis NA
Forced expiratory volume in 1-second (FEV1) -0.0171 0.00671 0.011 Wald ratio 1 cis NA
Diagnoses - main ICD10: N40 Hyperplasia of prostate -0.252 0.105 0.0166 Wald ratio 1 cis NA
Amygdala volume -22.8 10.1 0.0239 Wald ratio 1 cis NA
Pallidum volume -15.5 7.59 0.0414 Wald ratio 1 cis NA
Non-cancer illness code self-reported: hypertension 0.0259 0.0129 0.0442 Wald ratio 1 cis NA
Nucleus accumbens volume -9.21 4.66 0.0481 Wald ratio 1 cis NA
Diagnoses - main ICD10: K20 Oesophagitis 0.132 0.069 0.0556 Wald ratio 1 cis NA
Non-cancer illness code self-reported: asthma 0.039 0.0209 0.0626 Wald ratio 1 cis NA
…and 72 more outcomes (see JSON)              

2. pQTL instrument availability (Tier-B probe)

Dataset Trait Author Year
prot-c-4968_50_1 CAPG Suhre K 2019

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

37 association rows across 13 traits (37 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
AMBP/CAPG protein level ratio 2e-4277 rs6886 1 GCST90313252 no MR -> candidate analysis
Circulating CAPG levels 2e-789 rs2002444 3 GCST90860271 no MR -> candidate analysis
CAPG protein levels 7e-301 rs75000263 7 GCST90468537 no MR -> candidate analysis
Macrophage-capping protein levels 3e-207 rs62623452 4 GCST90248382 no MR -> candidate analysis
TGOLN2 protein levels 2e-143 rs11681965 14 GCST90470850 no MR -> candidate analysis
Cerebrospinal fluid protein CAPG levels 9e-90 rs6886 1 GCST90943116 no MR -> candidate analysis
platelet count (minimum, inv-norm transformed) 2e-25 rs62162752 1 GCST90480652 no MR -> candidate analysis
platelet count (mean, inv-norm transformed) 3e-25 rs62162752 1 GCST90480651 no MR -> candidate analysis
Platelet count 7e-18 rs3770102 1 GCST90662907 no MR -> candidate analysis
platelet count (maximum, inv-norm transformed) 1e-17 rs62162752 1 GCST90480650 no MR -> candidate analysis
Serum levels of protein CAPG 1e-10 rs35666320 1 GCST90088833 no MR -> candidate analysis
Diastolic blood pressure (MTAG) 2e-9 rs111384899 1 GCST90449057 no MR -> candidate analysis
…and 1 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 207 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
Sensorineural hearing impairment 0.584 common-variant locus no MR -> candidate analysis
cerebral atherosclerosis 0.041 common-variant locus no MR -> candidate analysis

Of the 2 rows above, 2 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 (Macrophage-capping protein)
gnomAD constraint pLI=2e-08, LOEUF=0.964 — LoF-tolerant
GWAS Catalog 111 unique SNPs / 256 rows
ClinVar 89 records; 0 pathogenic in sample of 30
PharmGKB/ClinPGx 1 clinical annotations across 1 drugs

Caveats declared by the tools

Sources

Provenance