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XB-GENEPAGE-963434
slc40a1 solute carrier family 40 (iron-regulated transporter), 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: slc40a1 assayed (12 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (19 sources): Abdominal pain, Anemia, Arrhythmia, Arthralgia, Cardiomyopathy, Cataract, Cirrhosis, Congenital hepatic fibrosis, Fatigue, Generalized hyperpigmentation, [+] |
Mouse (44 sources): abnormal enzyme/coenzyme level, abnormal forebrain development, abnormal macrophage physiology, abnormal pancreatic acinar cell morphology, abnormal spleen development, decreased body size, decreased bone mineral content, decreased circulating iron level, decreased circulating unsaturated transferrin level, decreased embryo size, [+] |
View all ortholog results at Monarch |