decreased circulating lactate level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced amount of lactate in the blood which is produced from pyruvate by lactate dehydrogenase (Mammalian Phenotype Ontology, MP_0013404)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013404
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Genes

8 gene mutations causing the decreased circulating lactate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CEBPD CCAAT/enhancer binding protein (C/EBP), delta
KLF15 Kruppel-like factor 15
OXCT1 3-oxoacid CoA transferase 1
PDK4 pyruvate dehydrogenase kinase, isozyme 4
PFKM phosphofructokinase, muscle
SLC13A5 solute carrier family 13 (sodium-dependent citrate transporter), member 5
SOD2 superoxide dismutase 2, mitochondrial
UCP2 uncoupling protein 2 (mitochondrial, proton carrier)