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XB-GENEPAGE-921720
slc2a3 solute carrier family 2 member 3
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: slc2a3 assayed (2 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (20 sources): Abnormality of eye movement, Abnormality of movement, Abnormality of the voice, Behavioral abnormality, Bradykinesia, Cerebellar atrophy, Cerebral cortical atrophy, Chorea, Dementia, Depression, [+] |
Mouse (13 sources): abnormal brain wave pattern, abnormal placental transport, behavior/neurological phenotype, decreased litter size, decreased prepulse inhibition, embryonic lethality between implantation and placentation, complete penetrance, growth/size/body region phenotype, homeostasis/metabolism phenotype, increased anxiety-related response, increased startle reflex, [+] |
View all ortholog results at Monarch |