About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Saraftm1c(KOMP)Wtsi
targeted mutation 1c, Wellcome Trust Sanger Institute
MGI:7509470
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Saraftm1c(KOMP)Wtsi/Saraftm1c(KOMP)Wtsi
Tg(Sim1-cre)1Lowl/0
involves: 129 * C57BL/6 * FVB MGI:7537120
cn2
Saraftm1c(KOMP)Wtsi/Saraftm1c(KOMP)Wtsi
Tg(Pgk1-cre)1Lni/0
involves: 129S4/SvJaeSor * BALB/c * C57BL/6J * C57BL/6N MGI:7537119


Genotype
MGI:7537120
cn1
Allelic
Composition
Saraftm1c(KOMP)Wtsi/Saraftm1c(KOMP)Wtsi
Tg(Sim1-cre)1Lowl/0
Genetic
Background
involves: 129 * C57BL/6 * FVB
Cell Lines EPD0613_2_B07
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Saraftm1c(KOMP)Wtsi mutation (0 available); any Saraf mutation (22 available)
Tg(Sim1-cre)1Lowl mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
N
• when fed a Western diet for 18 weeks, mice show no differences in total increase in body weight and composition relative to controls
• at 1 year, but not at 3 months, of age, percentage of lean mass is significantly higher than in control mice
• at 1 year, but not at 3 months, of age, body weight is significantly lower than that in control mice

adipose tissue
N
• at 1 year of age, inguinal and visceral adipose tissues show no differences in WAT droplet size relative to control mice; lipid accumulation phenotype is unchanged in Western diet-fed mice
• at 1 year of age, intracapsular brown adipose tissue (iBAT) shows significantly less fat accumulation (pixels of fat droplets/area) than in control mice
• at 1 year, but not at 3 months, of age, percentage of fat mass is significantly lower than in control mice

homeostasis/metabolism
N
• at 3 months of age, mice exhibit normal glucose tolerance relative to control mice
• when fed a Western diet for 18 weeks, mice show normal glucose tolerance and no differences in calorimetry relative to controls
• at 1 year of age, mice exhibit increased heat production over time and a significant increase in heat production per body weight

liver/biliary system
N
• mice show no fat accumulation in the liver at 1 year of age

behavior/neurological
• at 1 year of age, total food intake is not significantly altered, either under basal or refeed-challenged conditions; refeed responses are also unchanged in Western diet-fed mice
• at 3 months of age, mice do not exhibit altered anxiety-related behavioral phenotypes
• at 3 months and at 1 year of age, mice exhibit increased dark-phase locomotion, as indicated by the light beam breaks count




Genotype
MGI:7537119
cn2
Allelic
Composition
Saraftm1c(KOMP)Wtsi/Saraftm1c(KOMP)Wtsi
Tg(Pgk1-cre)1Lni/0
Genetic
Background
involves: 129S4/SvJaeSor * BALB/c * C57BL/6J * C57BL/6N
Cell Lines EPD0613_2_B07
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Saraftm1c(KOMP)Wtsi mutation (0 available); any Saraf mutation (22 available)
Tg(Pgk1-cre)1Lni mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• at 3 months and 1 year of age, percentage of lean mass is significantly lower than in control mice
• mice develop age-dependent sarcopenic obesity (not dependent on feeding or accompanied by diabetes)
• at 1 year of age, mice are overtly larger than control mice
• however, linear growth is not altered
• at 3 months of age, body weight is on average ~10% more than that in control mice
• by 1 year of age, body weight is nearly 20% more than that in controls

adipose tissue
• at 1 year of age, excess fat is distributed throughout the body with a high tendency for abdominal accumulation
• fat accumulates in intracapsular brown adipose tissue (iBAT), resulting in iBAT whitening by 1 year of age
• inguinal and visceral adipose tissues (iWAT and vWAT, respectively) show significant white fat cell hypertrophy at 3 months, with an upsurge noted at 1 year of age
• at 3 months and 1 year of age, percentage of fat mass is significantly higher than in control mice

liver/biliary system
• 1-year-old mice exhibit hepatic steatosis
• however, no fat accumulation is noted in the liver at 3 months of age
• primary hepatocytes isolated from 8- to 12-week-old mice show increased store-operated calcium entry (SOCE) activity, elevated Ca2+ oscillations in response to vasopressin (1 nM), and increased mitochondrial spare respiratory capacity

homeostasis/metabolism
N
• at 3 months of age, mice exhibit normal fasting glucose levels and normal glucose tolerance relative to control mice
• after 15 min of restraint stress, blood corticosterone levels are significantly higher than in control mice, suggesting an increase in hypothalamus-pituitary-adrenal (HPA) axis activation
• at 1 year of age, serum TSH levels are significantly higher than in control mice
• primary hepatocytes show increased store-operated calcium entry (SOCE) activity, and elevated Ca2+ oscillations in response to physiological levels of vasopressin (1 nM)
• at 3 months of age, mice exhibit a lower metabolic rate, with significantly decreased heat production over time

cellular
• primary mouse embryonic fibroblasts (MEFs) from E14.5 embryos show reduced proliferation relative to wild-type MEFs
• in the dorsal and the ventral hippocampus dentate gyrus, the number of PCNA-positive cells per doublecortin (DCX)-positive neuronal progenitors is significantly lower than in control mice
• primary hepatocytes exhibit an increased mitochondrial spare respiratory capacity

behavior/neurological
N
• at 3 months of age, total food intake is not significantly altered, either under basal or refeed-challenged conditions
• despite reduced neurogenesis, long-term memory (Morris water maze) and short-term memory (Y-maze) are unaffected
• 3-month-old mice spend more time in the lit compartment in the dark-light transfer test and show a longer reaction time in the first of three blocks of 120-db stimuli in the acoustic startle response assay, indicating reduced anxiety-like behavior
• at 3 months of age, mice exhibit reduced dark-phase locomotion, as indicated by the light beam breaks count

nervous system
• in the dorsal and the ventral hippocampus dentate gyrus, the number of PCNA-positive cells per doublecortin (DCX)-positive neuronal progenitors is significantly lower than in control mice
• EdU incorporation assays show a significant decrease in proliferation in the dorsal and the ventral hippocampus dentate gyrus

endocrine/exocrine glands
• at 1 year of age, mice exhibit subclinical hypothyroidism, with normal serum levels of thyroxine and cholesterol and increased serum TSH levels





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory