Bright Disease Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1704377
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Genes

29 genes associated with the disease Bright Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADM adrenomedullin
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
ALB albumin
CCL1 chemokine (C-C motif) ligand 1
CCL2 chemokine (C-C motif) ligand 2
CCL3 chemokine (C-C motif) ligand 3
CCL4 chemokine (C-C motif) ligand 4
CCL5 chemokine (C-C motif) ligand 5
CCL7 chemokine (C-C motif) ligand 7
CFD complement factor D (adipsin)
CXCL8 chemokine (C-X-C motif) ligand 8
CXCR3 chemokine (C-X-C motif) receptor 3
DES desmin
ESR1 estrogen receptor 1
FAS Fas cell surface death receptor
IFNG interferon, gamma
IL10 interleukin 10
IL18 interleukin 18
IL1B interleukin 1, beta
IL2 interleukin 2
IL2RA interleukin 2 receptor, alpha
IL6 interleukin 6
JUND jun D proto-oncogene
NGF nerve growth factor (beta polypeptide)
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
POMC proopiomelanocortin
PPARG peroxisome proliferator-activated receptor gamma
TNF tumor necrosis factor
WT1 Wilms tumor 1