abnormal glucose 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 glucose into the bloodstream (Mammalian Phenotype Ontology, MP_0001669)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001669
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4 gene mutations causing the abnormal glucose absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CD36 CD36 molecule (thrombospondin receptor)
CLOCK clock circadian regulator
FGFR2 fibroblast growth factor receptor 2
RSC1A1 regulatory solute carrier protein, family 1, member 1