abnormal thiamin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the concentration of thiamine (vitamin B1), a water soluble vitamin present in fresh vegetables and meats, especially liver (Mammalian Phenotype Ontology, MP_0011226)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011226
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1 gene mutations causing the abnormal thiamin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SLC19A3 solute carrier family 19 (thiamine transporter), member 3