tubular atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of renal tubules with thick redundant basement membranes, or a reduction of greater than 50% in tubular diameter compared to surrounding non-atrophic tubules. (Human Phenotype Ontology, HP_0000092)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000092
Similar Terms
Downloads & Tools


13 genes associated with the tubular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CEP83 centrosomal protein 83kDa
CLCN5 chloride channel, voltage-sensitive 5
GLIS2 GLIS family zinc finger 2
MUC1 mucin 1, cell surface associated
MYO1E myosin IE
NPHP1 nephronophthisis 1 (juvenile)
NPHP3 nephronophthisis 3 (adolescent)
NPHP4 nephronophthisis 4
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
REN renin
TMEM67 transmembrane protein 67
UMOD uromodulin
XPNPEP3 X-prolyl aminopeptidase 3, mitochondrial