Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (16) GO Terms (20) Nucleotides (44) Proteins (26) Interactants (45) Wiki
XB-GENEPAGE-855718

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