wagr syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A chromosomal disease that is a nephroblastoma that results_in a rare genetic syndrome in which affected children are predisposed to develop Wilms tumor, Aniridia (absence of the colored part of the eye, the iris), genitourinary anomalies, and mental retardation. The condition results from a deletion on chromosome 11 resulting in the loss of several genes. As such, it is one of the best studied examples of a condition caused by loss of neighbouring (contiguous) genes. (Human Disease Ontology, DOID_14515)
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Genes

25 genes co-occuring with the disease wagr syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
WT1 Wilms tumor 1 2.19563
PAX6 paired box 6 2.14993
PRRG4 proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane) 1.69542
FSHB follicle stimulating hormone, beta polypeptide 1.65879
MPPED2 metallophosphoesterase domain containing 2 1.32061
LIN7C lin-7 homolog C (C. elegans) 1.21175
KDM2B lysine (K)-specific demethylase 2B 1.08244
LGR4 leucine-rich repeat containing G protein-coupled receptor 4 1.04672
BDNF brain-derived neurotrophic factor 1.00203
LATS1 large tumor suppressor kinase 1 0.850354
KCNA4 potassium channel, voltage gated shaker related subfamily A, member 4 0.695905
CD151 CD151 molecule (Raph blood group) 0.608104
CRLF1 cytokine receptor-like factor 1 0.557509
CAT catalase 0.498085
RAG1 recombination activating gene 1 0.37555
KLF10 Kruppel-like factor 10 0.374068
SLC1A2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 0.352659
MECOM MDS1 and EVI1 complex locus 0.345675
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase) 0.30342
HBG2 hemoglobin, gamma G 0.297651
PTER phosphotriesterase related 0.255946
NPHS1 nephrosis 1, congenital, Finnish type (nephrin) 0.225573
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa 0.206248
MECP2 methyl CpG binding protein 2 0.195183
SRY sex determining region Y 0.178126