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XB-GENEPAGE-853954
ocln occludin
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (34 sources): Abnormality of movement, Anteverted nares, Axial hypotonia, Cataract, Cerebellar hypoplasia, Cerebral calcification, Cerebral cortical atrophy, Decreased liver function, Elevated circulating hepatic transaminase concentration, Failure to thrive, [+] |
Mouse (11 sources): abnormal basal ganglion morphology, abnormal gastric chief cell morphology, abnormal gastric parietal cell morphology, abnormal nursing, abnormal salivary gland duct morphology, abnormal seminiferous tubule morphology, abnormal stomach glandular epithelium morphology, abnormal stomach muscularis externa morphology, digestive/alimentary phenotype, homeostasis/metabolism phenotype, [+] |
View all ortholog results at Monarch |