Symbol
Name
ID

Galt
galactose-1-phosphate uridyl transferase
MGI:95638

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes

Abnormal erythrocyte enzyme concentration or activity

Reduced erythrocyte galactose-1-phosphate uridylyltransferase activity

Hypergalactosemia

Increased level of galactitol in plasma

Increased level of galactitol in red blood cells

Increased level of galactonate in red blood cells

Abnormal circulating enzyme concentration or activity

Elevated circulating hepatic transaminase concentration

Elevated circulating alanine aminotransferase concentration

Elevated circulating aspartate aminotransferase concentration

Hypoglycemia

Hyperchloremic metabolic acidosis

Metabolic acidosis

Food intolerance

Decreased circulating vitamin D concentration

Galactosuria

Increased level of galactitol in urine

Albuminuria

Aminoaciduria

Ascites

Decreased serum insulin-like growth factor 1

Disease(s) Associated with GALT

classic galactosemia

Mouse Phenotypes		cerebral edema	abnormal galactose homeostasis
Availability	Mouse Genotype	cerebral edema	abnormal galactose homeostasis
	Galt^{Gt(E285B04)Wrst}/Galt^{Gt(E285B04)Wrst}
	Galt^tm1Sgl/Galt^tm1Sgl

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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