renal glomerulus fibrosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description formation of fibrous tissue in the renal glomerulus as a result of repair or a reactive process (Mammalian Phenotype Ontology, MP_0011377)
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10 gene mutations causing the renal glomerulus fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CLU clusterin
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
MAN2C1 mannosidase, alpha, class 2C, member 1
MAS1 MAS1 proto-oncogene, G protein-coupled receptor
NOS3 nitric oxide synthase 3 (endothelial cell)
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
REN renin
RRM2B ribonucleotide reductase M2 B (TP53 inducible)
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B