renal glomerulus hypertrophy Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase in the bulk size of the capillary loops of the kidney that normally function as a filtration unit, due to cell enlargement (Mammalian Phenotype Ontology, MP_0011294)
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20 gene mutations causing the renal glomerulus hypertrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BAG6 BCL2-associated athanogene 6
BCL2 B-cell CLL/lymphoma 2
CD2AP CD2-associated protein
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
E2F2 E2F transcription factor 2
ESR1 estrogen receptor 1
FAS Fas cell surface death receptor
GDNF glial cell derived neurotrophic factor
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
GOLM1 golgi membrane protein 1
LEP leptin
LYN LYN proto-oncogene, Src family tyrosine kinase
MPV17 MpV17 mitochondrial inner membrane protein
NOS3 nitric oxide synthase 3 (endothelial cell)
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
PGAP3 post-GPI attachment to proteins 3
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
REN renin
VEGFA vascular endothelial growth factor A