abnormal response to vitamins Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description altered ability or inability to respond to or metabolize a group of organic substances that are required in trace amounts for the normal metabolic homeostasis of the body (Mammalian Phenotype Ontology, MP_0003639)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003639
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5 gene mutations causing the abnormal response to vitamins phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
KCP kielin/chordin-like protein
LASP1 LIM and SH3 protein 1
RARG retinoic acid receptor, gamma
TGIF1 TGFB-induced factor homeobox 1
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor