expanded mesangial matrix Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011353
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Genes

35 gene mutations causing the expanded mesangial matrix phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
APOE apolipoprotein E
ASIP agouti signaling protein
BCL2 B-cell CLL/lymphoma 2
BCL2L11 BCL2-like 11 (apoptosis facilitator)
CD151 CD151 molecule (Raph blood group)
CD2AP CD2-associated protein
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CFH complement factor H
CLU clusterin
COL18A1 collagen, type XVIII, alpha 1
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COL4A4 collagen, type IV, alpha 4
ESR1 estrogen receptor 1
FAS Fas cell surface death receptor
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
HPRT1 hypoxanthine phosphoribosyltransferase 1
INS insulin
ITGA1 integrin, alpha 1
KIRREL kin of IRRE like (Drosophila)
LCAT lecithin-cholesterol acyltransferase
LEP leptin
LEPR leptin receptor
MPV17 MpV17 mitochondrial inner membrane protein
MYO1E myosin IE
NOS3 nitric oxide synthase 3 (endothelial cell)
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
PDGFB platelet-derived growth factor beta polypeptide
PIK3C2A phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha
SCTR secretin receptor
SYK spleen tyrosine kinase
VEGFA vascular endothelial growth factor A
WAS Wiskott-Aldrich syndrome
WT1 Wilms tumor 1