abnormal vitamin e level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the concentration of vitamin E, tocopherol, including a series of eight structurally similar compounds; alpha-tocopherol is the most active form in humans and is a powerful biological antioxidant (Mammalian Phenotype Ontology, MP_0011231)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011231
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Genes

3 gene mutations causing the abnormal vitamin e level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PITPNA phosphatidylinositol transfer protein, alpha
PLTP phospholipid transfer protein
TTPA tocopherol (alpha) transfer protein