abnormality of urine glucose concentration Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the concentration of glucose in the urine. (Human Phenotype Ontology, HP_0011016)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011016
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Genes

24 genes associated with the abnormality of urine glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALDOB aldolase B, fructose-bisphosphate
ATP7B ATPase, Cu++ transporting, beta polypeptide
CLCN5 chloride channel, voltage-sensitive 5
COA5 cytochrome c oxidase assembly factor 5
COX10 COX10 heme A:farnesyltransferase cytochrome c oxidase assembly factor
COX14 COX14 cytochrome c oxidase assembly factor
COX20 COX20 cytochrome c oxidase assembly factor
COX6B1 cytochrome c oxidase subunit VIb polypeptide 1 (ubiquitous)
CTNS cystinosin, lysosomal cystine transporter
EHHADH enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase
ETFA electron-transfer-flavoprotein, alpha polypeptide
ETFB electron-transfer-flavoprotein, beta polypeptide
ETFDH electron-transferring-flavoprotein dehydrogenase
FAN1 FANCD2/FANCI-associated nuclease 1
FASTKD2 FAST kinase domains 2
GATA6 GATA binding protein 6
HNF1B HNF1 homeobox B
PET100 PET100 homolog (S. cerevisiae)
SLC16A12 solute carrier family 16, member 12
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2
SLC34A1 solute carrier family 34 (type II sodium/phosphate cotransporter), member 1
SLC5A1 solute carrier family 5 (sodium/glucose cotransporter), member 1
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
TACO1 translational activator of mitochondrially encoded cytochrome c oxidase I