| AAV | Adeno-associated virus |
| ATAC-seq | Assay for Transposase-Accessible Chromatin sequencing |
| BMP | Bone morphogenetic protein |
| CAKUT | Congenital anomalies of the kidney and urinary tract |
| CITED1 | Cbp/p300-interacting transactivator 1 |
| CKD | Chronic kidney disease |
| Cre | Causes recombination (recombinase) |
| CreERT2 | Tamoxifen-inducible Cre recombinase |
| CRISPR | Clustered regularly interspaced short palindromic repeats |
| CTNNB1 | Catenin beta 1 (β-catenin gene) |
| DNA | Deoxyribonucleic acid |
| ESRD | End-stage renal disease |
| ETS | E26 transformation-specific |
| ETV4/5 | ETS variant transcription factors 4/5 |
| EYA1 | Eyes absent homolog 1 |
| FDA | Food and Drug Administration |
| FGF | Fibroblast growth factor |
| FGFR | Fibroblast growth factor receptor |
| FOXD1 | Forkhead box D1 |
| GATA3 | GATA binding protein 3 |
| GDNF | Glial cell line-derived neurotrophic factor |
| GFRα1 | GDNF family receptor alpha 1 |
| HDR | Hypoparathyroidism, deafness, renal dysplasia (syndrome) |
| Hh | Hedgehog |
| HNF1B | Hepatocyte nuclear factor 1 beta |
| iPSC | Induced pluripotent stem cell |
| ITGA8 | Integrin subunit alpha 8 |
| JNK | c-Jun N-terminal kinase |
| loxP | Locus of X-over P1 |
| MAPK | Mitogen-activated protein kinase |
| MCDK | Multicystic dysplastic kidney |
| MET | Mesenchymal-to-epithelial transition |
| MM | Metanephric mesenchyme |
| NPC | Nephron progenitor cell |
| PAX2 | Paired box 2 |
| PBX1 | PBX homeobox 1 |
| PTCH1 | Patched 1 |
| PTEN | Phosphatase and tensin homolog |
| RET | Rearranged during transfection (receptor tyrosine kinase) |
| RNA | Ribonucleic acid |
| SALL1 | Spalt-like transcription factor 1 |
| scRNA-seq | Single-cell RNA sequencing |
| SIX2 | Sine oculis homeobox homolog 2 |
| SMAD | Suppressor of mothers against decapentaplegic |
| SPC | Stromal progenitor cell |
| SPRY1 | Sprouty RTK signaling antagonist 1 |
| TBX18 | T-box transcription factor 18 |
| TGF-β | Transforming growth factor beta |
| UB | Ureteric bud |
| UPJO | Ureteropelvic junction obstruction |
| VUR | Vesicoureteral reflux |
| WGS | Whole-genome sequencing |
| WNT | Wingless-related integration site |
| WT1 | Wilms tumor 1 |