Solute carrier family 1 member 5
SLC1A5geneSLC1A5 dysregulation in AMI impairs glutamate/cystine exchange, accelerating ferroptotic cardiomyocyte death.
Pathway placement
Cascade stepMyocardial injury (shared endpoint)
Confidencemedium
RationaleFerroptosis regulator; altered expression reflects ischemic cardiomyocyte amino-acid imbalance and death.
Druggability
DruggableYes
Known drugs / candidates0
Small-molecule tractableYes
Antibody tractableYes
EnsemblENSG00000105281
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
Literature evidence(1)
- Identification and characterization of novel ferroptosis-related genes in acute myocardial infarction.Human genomics · 2024 · PMID 39538299 · doi