absent digestive secretion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description failure to produce and/or release a physiologically active substance (usually but not exclusively in liquid form) from a cell or a gland of the digestive system (Mammalian Phenotype Ontology, MP_0000507)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000507
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1 gene mutations causing the absent digestive secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SLC26A9 solute carrier family 26 (anion exchanger), member 9