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XB-GENEPAGE-479124
slc4a4 solute carrier family 4 member 4
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: slc4a4 assayed (1 source) |
Computed annotations: slc4a4 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 (10 sources): Age-related nuclear cataract, Band keratopathy, Bicarbonate-wasting renal tubular acidosis, Cataract, Glaucoma, Growth delay, Hyperchloremic acidosis, Increased red cell osmotic resistance, Intellectual disability, Proximal renal tubular acidosis |
Mouse (34 sources): abnormal ammonia homeostasis, abnormal blood homeostasis, abnormal cranium morphology, abnormal intestine physiology, abnormal megakaryocyte morphology, abnormal renal reabsorption, abnormal renal tubule epithelium morphology, abnormal spleen B cell follicle morphology, acidemia, brittle teeth, [+] |
View all ortholog results at Monarch |