mesangial cell hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased number of the phagocytic cells in the capillary tuft of the renal glomerulus, interposed between endothelial cells and the basement membrane in the central or stalk region of the tuft (Mammalian Phenotype Ontology, MP_0011427)
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25 gene mutations causing the mesangial cell hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CD151 CD151 molecule (Raph blood group)
CD2AP CD2-associated protein
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CFH complement factor H
CLU clusterin
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COL4A5 collagen, type IV, alpha 5
FAS Fas cell surface death receptor
GADD45A growth arrest and DNA-damage-inducible, alpha
GDNF glial cell derived neurotrophic factor
HPRT1 hypoxanthine phosphoribosyltransferase 1
KIRREL kin of IRRE like (Drosophila)
LCAT lecithin-cholesterol acyltransferase
MARK2 MAP/microtubule affinity-regulating kinase 2
MTA2 metastasis associated 1 family, member 2
NFE2L2 nuclear factor, erythroid 2-like 2
NOS3 nitric oxide synthase 3 (endothelial cell)
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
PKN1 protein kinase N1
SYK spleen tyrosine kinase
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
TRAF3IP2 TRAF3 interacting protein 2
WAS Wiskott-Aldrich syndrome
WT1 Wilms tumor 1