Kidney renal clear cell carcinoma (KIRC) is a highly aggressive cancer. Disulfidptosis is a newly discovered mechanism of programmed cell death. However, the role of disulfidptosis-related lncRNAs (DRlncRNAs) in KIRC remains unknown. This study aimed to develop a prognostic model of DRlncRNAs and explore their prognostic value in KIRC. RNA-seq and relevant clinical data were obtained from The Cancer Genome Atlas (TCGA) database. Univariate Cox regression, lasso algorithm and multivariate Cox regression analysis identified DRlncRNAs and established a prognostic model. Multiple methods to assess the reliability of the model. In addition, Gene Set Enrichment Analysis (GSEA), immune infiltration analysis, somatic mutation analysis, and drug prediction were performed on the model. qRT-PCR has identified the intracellular expression of DRlncRNAs. We constructed a prognostic model with five DRlncRNAs and proved that the model was a good predictor of survival and prognosis of KIRC patients. GSEA indicated that DRlncRNAs were associated with apoptosis and immune-related pathways. Immune correlation analysis suggested that low-risk patients had better immunotherapeutic outcomes. Besides, somatic mutation analysis revealed that low-risk patients had a lower somatic mutation rate and TMB score and better prognostic. Drug prediction showed that axitinib, ibrutinib, osimertinib, and ruxolitinib were more effective in the low-risk patients; Crizotinib, lapatinib, linsitinib, and nilotinib were more effective in the high-risk patients. Finally, qRT-PCR confirmed the expression of DRlncRNAs in normal kidney cells and KIRC cell lines. In summary, we constructed a risk model and provided a new direction for diagnosing and treating KIRC.