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XB-GENEPAGE-483048
fxyd2 FXYD domain containing ion transport regulator 2
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: fxyd2 assayed (2 sources) |
Computed annotations: fxyd2 assayed (5 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (9 sources): Chondrocalcinosis, Generalized muscle weakness, Hypocalciuria, Hypokalemia, Hypomagnesemia, Myopia, Renal insufficiency, Renal magnesium wasting, Seizure |
Mouse (1 source): no abnormal phenotype detected |
View all ortholog results at Monarch |