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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Vgftm1Srjs
targeted mutation 1, Stephan R J Salton
MGI:2179681
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Vgftm1Srjs/Vgftm1Srjs B6.129-Vgftm1Srjs MGI:3828159
hm2
Vgftm1Srjs/Vgftm1Srjs involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:2449968
ht3
Vgftm1Srjs/Vgf+ B6.129-Vgftm1Srjs MGI:3828160


Genotype
MGI:3828159
hm1
Allelic
Composition
Vgftm1Srjs/Vgftm1Srjs
Genetic
Background
B6.129-Vgftm1Srjs
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Vgftm1Srjs mutation (0 available); any Vgf mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• unlike in mice with mixed background, locomotor activities are normal
• mice exhibit decreased freezing in a contextual fear conditioning assay compared to wild-type mice
• in a Morris water maze, mice exhibit increased latency to reach a hidden platform and travel a greater distance compared to wild-type mice
• however, swim speed and cued learning are normal

nervous system
• long term depression induced by low frequency stimulation is reduced compared to in wild-type mice

growth/size/body
• mice are lean compared to wild-type mice

adipose tissue
• fat stores are decreased compared to in wild-type mice

homeostasis/metabolism
• mice are hypermetabolic compared to wild-type mice




Genotype
MGI:2449968
hm2
Allelic
Composition
Vgftm1Srjs/Vgftm1Srjs
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Vgftm1Srjs mutation (0 available); any Vgf mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• survival of mutant mice was reduced in comparison to controls, particularly during the postnatal period prior to weaning

adipose tissue
• peripheral fat stores were dramatically reduced; total body fat was reduced and represented a smaller fraction of total body composition
• daily food intake was normal
• expression of leptin mRNA in the epididymal fat pad was significantly reduced

behavior/neurological
• hyperactivity was not associated with elevations in striatal dopamine or 3,4-dihydroxyphenylacetic (DOPAC) level
• the circadian period length was found to be slightly but significantly shorter in mutant animals

endocrine/exocrine glands
• 35% the weight of controls
• histological examination revealed many primary and atretic follicles but no mature follicles or corpus lutea
• ovaries weighed 18-30% less the weight of those found in wild-type mice
• 70% the weight of controls
• the mammary glands of postpartum females showed immature milk engorged ducts; pups born to mutant females failed to survive unless they fostered

growth/size/body
• mutants weighed 10-20% less than heterozygous littermates by postnatal day 3
• mutants weighed 40-60% less than heterozygous littermates by the third postnatal week
• after weaning, mutants maintained a body weight of 50-70% less than those of wildtype

homeostasis/metabolism
• reduced T4 thyroid hormone levels
• glucose levels measured 60% of levels found in controls
• serum corticosterone level was 140%
• serum insulin levels measured 80% of levels found in controls
• slightly decreased thyroid stimulating hormone (TSH) content
• mutant mice had an elevated basal metabolic rate as measured by oxygen consumption

reproductive system
• 35% the weight of controls
• histological examination revealed many primary and atretic follicles but no mature follicles or corpus lutea
• ovaries weighed 18-30% less the weight of those found in wild-type mice
• 70% the weight of controls
• oviducts weighed 18-30% less the weight of those found in wild-type mice
• uteri weighed 18-30% less the weight of those found in wild-type mice
• both males and females
• 50% of mutant females failed to cycle
• a prolonged pattern of up to 12 days was noted in 50% of mutant females
• females were responsive to superovulation
• 90% of mutant females (aged 8-12 weeks) were found to be infertile by virtue of nonproductive matings; fertility was restored by transplanting mutant ovaries into ovariectomized normal females, suggesting that the reproductive deficits were not due to primary ovarian pathology
• 85% of mutant males (aged 8-12 weeks) were found to be infertile by virtue of nonproductive matings; adult mating behavior was normal

nervous system
N
• hypothalamic structure and neuronal counts appeared normal

integument
• the mammary glands of postpartum females showed immature milk engorged ducts; pups born to mutant females failed to survive unless they fostered




Genotype
MGI:3828160
ht3
Allelic
Composition
Vgftm1Srjs/Vgf+
Genetic
Background
B6.129-Vgftm1Srjs
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Vgftm1Srjs mutation (0 available); any Vgf mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice exhibit decreased freezing in a contextual fear conditioning assay compared to wild-type mice





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory