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XB-GENEPAGE-1011740
slc39a8 solute carrier family 39 (zinc transporter), member 8
Expression Phenotypes
Gene expression phenotype annotations where the gene of interest has been
disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from
differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1,
FDR <= 0.05 and an absolute LogFC >= 2.
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Computed annotations: slc39a8 assayed (6 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (47 sources): Abnormal blood zinc concentration, Abnormality of the liver, Astigmatism, Cerebellar atrophy, Cerebral atrophy, Cerebral cortical atrophy, Craniosynostosis, Cutaneous syndactyly of toes, Decreased activity of mitochondrial complex II, Decreased activity of mitochondrial complex IV, [+] |
Mouse (5 sources): abnormal zinc level, increased fetal cardiomyocyte proliferation, lethality throughout fetal growth and development, complete penetrance, preweaning lethality, complete penetrance, thin myocardium compact layer |
View all ortholog results at Monarch |