CoronaryAtlas logo
CoronaryAtlas
Sodium-glucose co-transporter 2
Pathway / Off-pathway / systemic markers

Sodium-glucose co-transporter 2

SLC5A2gene

Renal electrolyte handling with indirect MI risk via glycemic control, not atherothrombotic pathway.

Pathway placement
Cascade stepOff-pathway / systemic markers
Confidencehigh
RationaleRenal glucose reabsorption; glycemic/systemic risk factor; off-pathway.
Druggability
DruggableYes
Known drugs / candidates17
Small-molecule tractableYes
Antibody tractableYes
EnsemblENSG00000140675

Type I vs non-Type I discrimination

ScoresIndeterminate
R — rupture / Type-I
C — non-Type-I
0
A — assay feasibility
52
E — evidence strength
50
T1DI (composite)
15
Specificity differential (R−C)+15
Non-Type-I axis panel
Does this marker also move in each non-Type-I setting? mag 0–3; higher means less Type-I-specific. n/a = no evidence retrieved, which is not the same as no change.
2sepsis / systemic inflammationn/a
2anemia / acute blood lossn/a
2hypovolemia / dehydrationmag 0
2tachyarrhythmian/a
2hypoxemia / respiratory failuren/a
2hypertensive emergencyn/a
2high-demand / peri-operative stressn/a
3sudden cardiac deathn/a
4aPCI-related periproceduraln/a
4bstent thrombosisn/a
4cin-stent restenosisn/a
5CABG-relatedn/a
Coverage: 1/12 axes with evidence
Tier: deep-scored (abstract-extracted) · 1 supporting references. See the discrimination table for all markers.

Assay & specimen

Class-level default (no specific cleared assay)— generic method inferred from analyte class; confirm against a specific product insert before use.
Specimen
Whole blood — gene is not a circulating analyte; measure protein product or genotype
Collection tube
K2-EDTA whole blood (lavender-top)
Method / principle
SNP genotyping / sequencing; or immunoassay of encoded protein
Reagent / substrate
Allele-specific primers/probes (TaqMan) or NGS panel; or antibody for protein
Platform
qPCR / NGS / array
Turnaround · availability
Send-out · Genotyping widely available; protein assay variable

Human genetic evidence

0.352
Open Targets association (acute_MI)

Literature evidence(0)

No direct literature mentions harvested; included via genetic/target evidence.