slc2a2 Phenotypes

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Phenotypes

Gene Literature (55)

Nucleotides (244)

Interactants (420)

XB-GENEPAGE-486461

Gene Symbol: slc2a2 Gene Name: solute carrier family 2 member 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.
Computed annotations: slc2a2 assayed (22 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (18 sources): Abdominal distention, Acidosis, Chronic acidosis, Elevated circulating alkaline phosphatase concentration, Failure to thrive, Generalized aminoaciduria, Global developmental delay, Glycosuria, Hyperphosphaturia, Hypokalemia, Hypophosphatemia, Hypouricemia, Impairment of galactose metabolism, Malabsorption, Osteomalacia, Poor appetite, Reduced subcutaneous adipose tissue, Renal tubular dysfunction [+]
Mouse (18 sources): abnormal bile salt level, abnormal glycogen homeostasis, abnormal lipid homeostasis, abnormal pancreatic islet morphology, cardiovascular system phenotype, decreased cellular glucose uptake, decreased insulin secretion, decreased liver cholesterol level, decreased liver triglyceride level, decreased pancreas weight, decreased pancreatic beta cell mass, homeostasis/metabolism phenotype, increased blood osmolality, increased fatty acids level, increased muscle cell glucose uptake, increased pancreatic alpha cell mass, postnatal lethality, complete penetrance, preweaning lethality, complete penetrance [+]
View all ortholog results at Monarch