lipoid nephrosis Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

30 genes co-occuring with the disease lipoid nephrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
POMC proopiomelanocortin 1.40483
CD79A CD79a molecule, immunoglobulin-associated alpha 1.09629
CFP complement factor properdin 0.766351
MX2 MX dynamin-like GTPase 2 0.696306
ANGPTL4 angiopoietin-like 4 0.582384
LMX1B LIM homeobox transcription factor 1, beta 0.579272
UBC ubiquitin C 0.568775
ACTN4 actinin, alpha 4 0.567997
RPS27A ribosomal protein S27a 0.55945
ETV4 ets variant 4 0.512648
UBB ubiquitin B 0.511496
VEGFA vascular endothelial growth factor A 0.475255
ALB albumin 0.434148
SDC2 syndecan 2 0.406798
RRM1 ribonucleotide reductase M1 0.391885
LIG3 ligase III, DNA, ATP-dependent 0.38111
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin) 0.372587
MX1 MX dynamin-like GTPase 1 0.31464
F12 coagulation factor XII (Hageman factor) 0.292257
CXCL8 chemokine (C-X-C motif) ligand 8 0.282225
IL10 interleukin 10 0.27687
IL13 interleukin 13 0.269043
LYZ lysozyme 0.254536
NPHS1 nephrosis 1, congenital, Finnish type (nephrin) 0.253479
REN renin 0.251366
HMGA2 high mobility group AT-hook 2 0.241196
MMP14 matrix metallopeptidase 14 (membrane-inserted) 0.234573
CD276 CD276 molecule 0.222136
F8 coagulation factor VIII, procoagulant component 0.204923
CR1 complement component (3b/4b) receptor 1 (Knops blood group) 0.163938