CausalSentinel

Protein Dossier — CD200R1 (Cell surface glycoprotein CD200 receptor 1)

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: asthma 0.15 0.0336 8.51e-06 Wald ratio 1 cis NA
Non-cancer illness code self-reported: hypopituitarism 0.979 0.319 0.00215 Wald ratio 1 cis NA
Diagnoses - main ICD10: I80 Phlebitis and thrombophlebitis 0.415 0.138 0.00255 Wald ratio 1 cis NA
Eczema 0.288 0.0972 0.00307 Wald ratio 1 cis NA
Non-cancer illness code self-reported: pernicious anaemia 0.477 0.164 0.00369 Wald ratio 1 cis NA
Diagnoses - main ICD10: I48 Atrial fibrillation and flutter 0.285 0.1 0.00444 Wald ratio 1 cis NA
Non-cancer illness code self-reported: hayfever or allergic rhinitis 0.133 0.0502 0.00834 Wald ratio 1 cis NA
Cancer code self-reported: basal cell carcinoma 0.286 0.111 0.00971 Wald ratio 1 cis NA
Serum creatinine (eGFRcrea) 0.0125 0.00523 0.0168 Wald ratio 1 cis NA
Non-cancer illness code self-reported: pneumothorax 0.795 0.355 0.0253 Wald ratio 1 cis NA
Diagnoses - main ICD10: R07 Pain in throat and chest 0.114 0.0555 0.04 Wald ratio 1 cis NA
Diagnoses - main ICD10: S76 Injury of muscle and tendon at hip and thigh level 0.743 0.366 0.0424 Wald ratio 1 cis NA
…and 94 more outcomes (see JSON)              

2. pQTL instrument availability (Tier-B probe)

Dataset Trait Author Year
prot-c-5103_30_3 MO2R1 Suhre K 2019

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

37 association rows across 22 traits (34 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 CD200R1 levels 4e-3173 rs79556290 3 GCST90859738 no MR -> candidate analysis
CD200R1 protein levels 1e-270 rs4682447 4 GCST90468605 no MR -> candidate analysis
Cell surface glycoprotein CD200 receptor 1 levels 4e-174 rs77561169 3 GCST90059915 no MR -> candidate analysis
Cerebrospinal fluid protein CD200R1 levels 5e-59 rs57891445 1 GCST90943148 no MR -> candidate analysis
Neurological blood protein biomarker levels 2e-30 rs79834152 2 GCST008478 no MR -> candidate analysis
Atopic dermatitis 5e-29 rs6808249 2 GCST90244787 no MR -> candidate analysis
Eosinophil percentage of white cells 9e-23 rs35297201 1 GCST90002382 no MR -> candidate analysis
Eosinophil count 2e-22 rs12494693 4 GCST90002381 no MR -> candidate analysis
Height 9e-21 rs7432373 1 GCST90245848 MR: beta=-0.0239, p=0.162 (cis)
CD200 protein levels 2e-19 rs1488193 1 GCST90468606 no MR -> candidate analysis
Eosinophill count (UKB data field 30150) 4e-19 rs12494693 1 GCST90468068 no MR -> candidate analysis
Circulating CD200 levels 6e-18 rs55664715 1 GCST90859700 no MR -> candidate analysis
…and 10 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 294 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
asthma 0.667 common-variant locus MR: beta=0.15, p=8.51e-06 (cis)
atopic eczema 0.668 common-variant locus no MR -> candidate analysis
hypothyroidism 0.669 common-variant locus MR: beta=0.0725, p=0.209 (cis)
dermatitis 0.667 common-variant locus no MR -> candidate analysis
Eczematoid dermatitis 0.55 common-variant locus no MR -> candidate analysis
alcohol drinking 0.466 common-variant locus no MR -> candidate analysis
corneal neovascularization 0.134 common-variant locus no MR -> candidate analysis
device complication 0.12 common-variant locus no MR -> candidate analysis

Of the 8 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 not available — no ChEMBL target (undrugged)
gnomAD constraint pLI=8.7e-09, LOEUF=1.07 — LoF-tolerant
GWAS Catalog 50 unique SNPs / 100 rows
ClinVar 89 records; 0 pathogenic in sample of 30
PharmGKB/ClinPGx no annotations

Caveats declared by the tools

Sources

Provenance