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XB-GENEPAGE-1003483
slc7a9 solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9
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: slc7a9 assayed (3 sources) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Human (11 sources): Abnormality of amino acid metabolism, Abnormality of the nervous system, Argininuria, Cystinuria, Hematuria, Hyperlysinuria, Hyperuricemia, Nephrolithiasis, Ornithinuria, Recurrent urinary tract infections, [+] |
| Mouse (6 sources): abnormal renal tubule morphology, crystalluria, dilated renal tubules, increased urinary bladder weight, renal cast, urolithiasis |
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View all ortholog results at Monarch |