renal glycosuria Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_9432)
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Genes

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

Symbol Name Standardized Value
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2 1.67638
CLCNKA chloride channel, voltage-sensitive Ka 1.13163
SLC5A1 solute carrier family 5 (sodium/glucose cotransporter), member 1 1.12572
SLC5A4 solute carrier family 5 (glucose activated ion channel), member 4 0.96918
TREH trehalase (brush-border membrane glycoprotein) 0.858134
BSND barttin CLCNK-type chloride channel accessory beta subunit 0.799923
INS insulin 0.797872
CLCNKB chloride channel, voltage-sensitive Kb 0.67551
POMC proopiomelanocortin 0.669936
CLCN5 chloride channel, voltage-sensitive 5 0.632777
NOS1 nitric oxide synthase 1 (neuronal) 0.577327
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1 0.541605
PHEX phosphate regulating endopeptidase homolog, X-linked 0.531154
TES testin LIM domain protein 0.500761
SLC5A7 solute carrier family 5 (sodium/choline cotransporter), member 7 0.443171
AVP arginine vasopressin 0.42364
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2 0.381481
B2M beta-2-microglobulin 0.356341
HNF1A HNF1 homeobox A 0.342006
HK1 hexokinase 1 0.298371
FBXL20 F-box and leucine-rich repeat protein 20 0.282225
HBB hemoglobin, beta 0.26266
FGF23 fibroblast growth factor 23 0.207578
ACTB actin, beta 0.202618
ACTG1 actin gamma 1 0.178126