Childhood Nephrotic Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C3874381
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Genes

20 genes associated with the disease Childhood Nephrotic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ABCC1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1
APOE apolipoprotein E
CD14 CD14 molecule
CD9 CD9 molecule
HDAC2 histone deacetylase 2
HLA-G major histocompatibility complex, class I, G
HP haptoglobin
IL12B interleukin 12B
IL13 interleukin 13
IL1RN interleukin 1 receptor antagonist
IL4 interleukin 4
MDM4 MDM4, p53 regulator
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
MSH3 mutS homolog 3
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
POMC proopiomelanocortin
TBC1D9 TBC1 domain family, member 9 (with GRAM domain)
TGFB1 transforming growth factor, beta 1
TNF tumor necrosis factor