abnormal fructose absorption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the ability of the small intestine to absorb fructose into the bloodstream (Mammalian Phenotype Ontology, MP_0001668)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001668
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1 gene mutations causing the abnormal fructose absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SLC2A8 solute carrier family 2 (facilitated glucose transporter), member 8