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XB-GENEPAGE-489633
slc25a3 solute carrier family 25 member 3
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (13 sources): Abnormal mitochondrial shape, Abnormality of the mitochondrion, Cyanosis, Failure to thrive, Hypertrophic cardiomyopathy, Hypotonia, Increased serum lactate, Lactic acidosis, Low-output congestive heart failure, Metabolic acidosis, [+] |
Mouse (17 sources): abnormal allantois morphology, abnormal calcium ion homeostasis, abnormal cardiac muscle tissue morphology, abnormal channel response, abnormal embryo turning, abnormal heart looping, abnormal limb bud morphology, abnormal mitochondrial ATP synthesis coupled electron transport, abnormal optic vesicle formation, abnormal otic vesicle morphology, [+] |
View all ortholog results at Monarch |