impaired cellular glucose import Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced ability of a cell to take in glucose from the environment (Mammalian Phenotype Ontology, MP_0003926)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003926
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Genes

3 gene mutations causing the impaired cellular glucose import phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MGAT4A mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme A
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
TXNIP thioredoxin interacting protein