slc26a3.1 solute carrier family 26, member 3, gene 1
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
|Human (16 sources): Abdominal distention, Abnormality of the cardiovascular system, Alkalosis, Dehydration, Diarrhea, Failure to thrive, Growth abnormality, Growth delay, Hyperactive renin-angiotensin system, Hyperaldosteronism, [+]|
|Mouse (6 sources): abnormal colon morphology, abnormal feces composition, abnormal large intestine crypts of Lieberkuhn morphology, increased cell proliferation, postnatal lethality, incomplete penetrance, premature death|
View all ortholog results at Monarch