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XB-GENEPAGE-479768
eomes eomesodermin
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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Manual annotations: eomes assayed (5 sources) |
Computed annotations: eomes manipulated (3 sources), eomes assayed (29 sources) |
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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Xtr Wt + vegt MO + eomes MO + tbxt MO + tbxt.2 MO (3 sources), Xtr Wt + eomes + animal cap explant (0 sources), Xtr Wt + foxb1 + eomes + animal cap explant (0 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (7 sources): Agenesis of corpus callosum, Cerebellar hypoplasia, Polymicrogyria, Primary microcephaly, Recurrent infections, Respiratory distress, Ventriculomegaly |
Mouse (45 sources): abnormal anterior primitive streak morphology, abnormal axon guidance, abnormal dentate gyrus morphology, abnormal egg cylinder morphology, abnormal embryonic epiblast morphology, abnormal leukocyte migration, abnormal neuron apoptosis, abnormal neuronal precursor proliferation, abnormal primitive streak elongation, abnormal primitive streak morphology, [+] |
View all ortholog results at Monarch |