abnormal zinc homeostasis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the processes involved in the maintenance of an internal equilibrium of zinc that normally is a cofactor in many proteins (Mammalian Phenotype Ontology, MP_0009615)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009615
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Genes

6 gene mutations causing the abnormal zinc homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SLC30A3 solute carrier family 30 (zinc transporter), member 3
SLC30A4 solute carrier family 30 (zinc transporter), member 4
SLC30A7 solute carrier family 30 (zinc transporter), member 7
SLC30A8 solute carrier family 30 (zinc transporter), member 8
SLC39A14 solute carrier family 39 (zinc transporter), member 14
SLC39A5 solute carrier family 39 (zinc transporter), member 5