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. 2015 Oct 20;3:65. doi: 10.3389/fcell.2015.00065

Table 1.

Proteins found in human urinary exosomes that are specific to or enriched in given regions of the kidney.

Kidney region Gene symbol Full gene name Species Exosome sample Identified molecule Associated diseases
Glomerulus PODXL Podocalyxin-like Protein Homo sapiens Urine Protein Diabetic nephropathy
NPHS2 Podocin Homo sapiens Urine mRNA Focal segmental glomerulosclerosis, nephrotic syndrome [MIM: 600995]
LGALS1 Galectin-1 Homo sapiens Urine mRNA
HSPG2 Heparan Sulfate Proteoglycan 2 Homo sapiens Urine mRNA Schwartz-Jampel syndrome type 1 [MIM: 255800]
1st convoluted tubule gp330 precursor Glycoprotein 330 Precursor Homo sapiens Urine Protein Renal aminoglycoside accumulation and nephrotoxicity, Donnai-Barrow syndrome
CUBN Cubilin (Intrinsic Factor-Cobalamin Receptor) Homo sapiens Urine Protein, mRNA Megaloblastic anemia 1 [MIM: 261100]
AQP1 Aquaporin1 Homo sapiens Urine protein, mRNA Nephrogenic diabetes insipidus, Aquaporin 1 deficiency, Colton-Null [MIM: 110450]
LRP2 Megalin Homo sapiens Urine mRNA Heymann nephritis, proteinuria
CA4 Carbonic Anhydrase 4 Homo sapiens Urine mRNA Diabetic nephropathy, Proximal renal tubular acidosis [MIM: 114760]
ANPEP Alanyl Aminopeptidase Homo sapiens Urine protein Hypertension [MIM: 151530]
NAPSA NapsinA Homo sapiens Urine Protein Kidney carcinoma, renal neoplasms
CLCN 5 Chloride Channel Protein 5 Homo sapiens Urine mRNA Dent's disease
GGT1 γ-glutamyltransferase Homo sapiens (male) Urine Protein
APN Aminopeptidase N Homo sapiens (male) Urine Protein
Henle's loop AQP1 Aquaporin 1 Homo sapiens Urine Protein Nephrogenic diabetes insipidus, Aquaporin 1 deficiency, Colton-Null [MIM: 110450]
UMOD Uromodulin Homo sapiens Urine Protein Hyperuricemic nephropathy, Medullary cystic kidney disease-2 (MCKD2) [MIM: 603860], familial juvenile hyperuricemic nephropathy (FJHN) [MIM: 16200]
THP Tamm-Horsfall Protein Homo sapiens (male) Urine Protein Mckd2 [mim: 603860], fjhn [mim: 16200]
CD9 Cluster of Differentiation (Tetraspanin) Homo sapiens (male) Urine Protein
BDKRB1 Bradykinin B1 Receptor Homo sapiens Urine mRNA
CALCR Calcitonin Receptor Homo sapiens Urine mRNA Kidney stone disease
SCNN1D Amiloride-sensitive Sodium Channel Subunit Delta Homo sapiens Urine mRNA
2nd convoluted tubule SLC12A3 (NCC) Thiazide-sensitive Na-Cl Cotransporter Homo sapiens Urine Protein Gitelman syndrome [MIM: 263800]
Collecting ducts AQP2 Aquaporin 2 Homo sapiens Urine mRNA Nephrogenic diabetes insipidus type 1 [MIM: 222000] [MIM: 125800]
ATP6V1B1 V-ATPase B1 Subunit Homo sapiens Urine mRNA Distal renal tubular acidosis [MIM: 267300]
SLC12A1 Kidney-specific Na-K-Cl Symporter Homo sapiens Urine mRNA Bartter-Syndrome type 1, 2, 3 [MIM: 601678, 241200, 607364]
MUC1 Mucin-1 Homo sapiens (male) Urine Protein Renal cell carcinoma, Medullary cystic kidney disease type 1 (MCKD1) [MIM:174000]
RHCG Rh type C glycoprotein Homo sapiens (male) Urine Protein

Data compiled from Pisitkun et al. (2004), Gonzales et al. (2009), Miranda et al. (2010), Dear et al. (2013), and Musante et al. (2014) and the Online Mendelian. Inheritance in Man OMIM® website (http://www.omim.org/, see MIM numbers for reference).