abnormal glomerular filtration rate Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly in the volume of water filtered out of plasma through glomerular capillary walls into Bowman's capsules per unit of time. (Human Phenotype Ontology, HP_0012212)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012212
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Genes

6 genes associated with the abnormal glomerular filtration rate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BSND barttin CLCNK-type chloride channel accessory beta subunit
CLCNKA chloride channel, voltage-sensitive Ka
CLCNKB chloride channel, voltage-sensitive Kb
G6PC glucose-6-phosphatase, catalytic subunit
MUC1 mucin 1, cell surface associated
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
Funding