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XB-GENEPAGE-1011543
slc1a1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
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: slc1a1 assayed (13 sources) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Human (5 sources): Aminoaciduria, Aspartic aciduria, Fasting hypoglycemia, Intellectual disability, Nephrolithiasis |
| Mouse (15 sources): abnormal circulating iron level, abnormal circulating sodium level, abnormal response to new environment, behavior/neurological phenotype, decreased locomotor activity, decreased retina ganglion cell number, fused cornea and lens, increased cellular sensitivity to hydrogen peroxide, increased circulating iron level, increased exploration in new environment, [+] |
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View all ortholog results at Monarch |