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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Slc17a6tm1Lowl
targeted mutation 1, Bradford B Lowell
MGI:3771177
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Slc17a6tm1Lowl/Slc17a6tm1Lowl
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Nr5a1-cre)2Lowl/0
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * FVB MGI:4442973


Genotype
MGI:4442973
cn1
Allelic
Composition
Slc17a6tm1Lowl/Slc17a6tm1Lowl
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Nr5a1-cre)2Lowl/0
Genetic
Background
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slc17a6tm1Lowl mutation (2 available); any Slc17a6 mutation (60 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
Tg(Nr5a1-cre)2Lowl mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue
• when fed a high fat diet, mice exhibit a slight increase in fat stores

behavior/neurological
• when fed a high fat diet, mice exhibit a slight increase in food intake

growth/size/body
• when fed a high fat diet, mice exhibit a slight increase in fat stores
• mice exhibit a greater increase in weight when fed a high fat diet compared to wild-type mice

homeostasis/metabolism
• after a 24 hour fast, mice exhibit decreased blood glucose levels (males, 55+/-3 compared to 68+/-5 mg/dl in wild-type mice; females 53+/-2 compared to 67+/-5 mg/dl in wild-type mice)
• acute administration of insulin induces hypoglycemia
• mice exhibit impaired fasting-mediated increase in pancreatic hormone glucagon
• following hypoglycemia, mice fail to exhibit an increase in plasma epinephrine levels
• during fasting and following hypoglycemia, mice fail to exhibit an increase in plasma glucagons compared to wild-type mice
• glucose plasma levels fail to increase following central administration of 2-deoxyglucose as in wild-type mice
• however, the hyperhagic response initiated by central administration of 2-deoxyglucose is normal

nervous system
• neurons do not possess any glutamatergic excitatory postsynaptic current





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory