Renal dysfunction in dogs envenomed by snakes has mostly been evaluated using routine serum and urine renal markers. Generally, these are not able to detect the renal damage at an early stage and their sensitivity is affected by hemolysis, hematuria and pigmenturia. Selective use of urinary biomarkers can provide early information on severity and stage of renal injury caused by nephrotoxic substances before major decline in renal function occurs. Therefore, the aim of this study was to evaluate venom-induced renal damage using urinary markers of glomerular (urinary albumin (uAlb), immunoglubin G (IgG) and Creactive protein (uCRP)) and proximal tubular dysfunction (urinary retinol binding protein (uRBP)) and compare these markers with routine renal markers (serum urea (BUN) and creatinine (sCr), urinary specific gravity (USG) and urinary protein to creatinine ratio (UPC)).Nineteen dogs envenomed by either neurotoxic or cytotoxic snakes and ten clinically healthy dogs were included in this study. Urinary markers were measured using previously validated commercially available ELISA kits. Among measured routine renal markers a significant difference between snake -envenomed and healthy dogs was noted only in UPC, but in the presence of hematuria and hemoglobinuria, differentiation between prerenal and renal proteinuria was not possible. The urinary biomarkers uAlb, uIgG and uRBP in snakeenvenomed dogs were significantly increased (P<0.05) when compared to healthy dogs at admission, whereas 24 h after envenomation only uCRP was significantly elevated. Using urinary /markers, results of this study showed that snake venom evokes renal dysfunction at the glomerular and tubular region of the nephron.