abnormal cardiac cell glucose uptake Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalous ability of the cells of the heart to take in glucose (Mammalian Phenotype Ontology, MP_0004039)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004039
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7 gene mutations causing the abnormal cardiac cell glucose uptake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CD36 CD36 molecule (thrombospondin receptor)
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
FABP3 fatty acid binding protein 3, muscle and heart
LMBRD1 LMBR1 domain containing 1
THRA thyroid hormone receptor, alpha
THRB thyroid hormone receptor, beta
TXNIP thioredoxin interacting protein