abnormal renal glucose reabsorption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the process in which glucose is taken up from the collecting ducts and proximal and distal loops of the nephron (Mammalian Phenotype Ontology, MP_0011447)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011447
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4 gene mutations causing the abnormal renal glucose reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
HNF1A HNF1 homeobox A
PHEX phosphate regulating endopeptidase homolog, X-linked
SLC5A1 solute carrier family 5 (sodium/glucose cotransporter), member 1
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2