abnormal vitamin absorption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the ability to take in any of a group of organic substances, present in food, that are essential to normal metabolism (Mammalian Phenotype Ontology, MP_0001671)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001671
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4 gene mutations causing the abnormal vitamin absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PITPNA phosphatidylinositol transfer protein, alpha
RBP2 retinol binding protein 2, cellular
SLC19A3 solute carrier family 19 (thiamine transporter), member 3
SLC23A1 solute carrier family 23 (ascorbic acid transporter), member 1