remittent intestinal hemorrhage Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description loss of blood from the intestines that is characterized by temporary periods of abatement (Mammalian Phenotype Ontology, MP_0000510)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000510
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Genes

1 gene mutations causing the remittent intestinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2