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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Slc2a9
solute carrier family 2 (facilitated glucose transporter), member 9
MGI:2152844
49 phenotypes from 3 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Slc2a9tm1.1Thor/Slc2a9+
Albtm1(cre/ERT2)Mtz/Alb+
involves: 129S2/SvPas * C57BL/6 * C57BL/6N 		increased urine magnesium level J:153089
increased urine phosphate level J:153089
Slc2a9tm1.1Thor/Slc2a9tm1.1Thor
Albtm1(cre/ERT2)Mtz/Alb+
involves: 129S2/SvPas * C57BL/6 * C57BL/6N 		decreased urine osmolality J:153089
decreased urine pH J:153089
increased blood uric acid level J:153089
increased urine magnesium level J:153089
increased urine phosphate level J:153089
increased urine potassium level J:153089
polyuria J:153089
normal renal/urinary system phenotype J:153089
uraturia J:153089
Slc2a9tm1.2Thor/Slc2a9+
involves: C57BL/6 * C57BL/6N 		increased circulating magnesium level J:153089
increased urine sodium level J:153089
Slc2a9tm1.2Thor/Slc2a9tm1.2Thor
involves: C57BL/6 * C57BL/6N 		abnormal renal reabsorption J:153089
decreased body weight J:153089
decreased urine osmolality J:153089
decreased urine pH J:153089
dilated renal tubule J:153089
hydronephrosis J:153089
increased blood uric acid level J:153089
increased circulating creatinine level J:153089
increased circulating magnesium level J:153089
increased urine magnesium level J:153089
increased urine potassium level J:153089
increased urine sodium level J:153089
kidney cortex atrophy J:153089
kidney cortex cyst J:153089
kidney inflammation J:153089
nephrolithiasis J:153089
polydipsia J:153089
polyuria J:153089
prenatal lethality, incomplete penetrance J:153089
renal interstitial fibrosis J:153089
renal tubule atrophy J:153089
tubulointerstitial nephritis J:153089
uraturia J:153089
Slc2a9tm1Khm/Slc2a9tm1Khm
involves: 129 * C57BL/6 		no abnormal phenotype detected J:221544
Slc2a9tm1Khm/Slc2a9tm1Khm
Tg(Vil1-cre)997Gum/0
involves: 129 * C57BL/6 * C57BL/6J 		abnormal circulating lipid level J:221544
abnormal enterocyte physiology J:221544
abnormal feces composition J:221544
abnormal heart echocardiography feature J:221544
abnormal metabolism J:221544
decreased respiratory quotient J:221544
hepatic steatosis J:221544
hypertension J:221544
increased basal metabolism J:221544
increased blood uric acid level J:221544
increased body fat mass J:221544
increased circulating cholesterol level J:221544
increased circulating free fatty acids level J:221544
increased circulating insulin level J:221544
increased circulating triglyceride level J:221544
increased energy expenditure J:221544
increased heart rate J:221544
increased liver free fatty acids level J:221544
increased liver triglyceride level J:221544
increased oxygen consumption J:221544
increased percent body fat/body weight J:221544
increased urine uric acid level J:221544
insulin resistance J:221544
liver fibrosis J:221544
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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Send questions and comments to User Support. 		last database update
04/30/2024
MGI 6.23 		The Jackson Laboratory