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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Socs2tm1Wehi
targeted mutation 1, Walter and Eliza Hall Institute of Medical Research
MGI:1934557
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Socs2tm1Wehi/Socs2tm1Wehi C57BL/6-Socs2tm1Wehi MGI:3808597
hm2
Socs2tm1Wehi/Socs2tm1Wehi involves: C57BL/6 * C57BL/6J MGI:5431237
ht3
Socs2tm1Wehi/Socs2+ C57BL/6-Socs2tm1Wehi MGI:3808832
cx4
Phf6tm1.2Avo/Y
Socs2tm1Wehi/Socs2tm1Wehi
involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N MGI:6507212


Genotype
MGI:3808597
hm1
Allelic
Composition
Socs2tm1Wehi/Socs2tm1Wehi
Genetic
Background
C57BL/6-Socs2tm1Wehi
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Socs2tm1Wehi mutation (0 available); any Socs2 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• at 6 weeks of age, male homozygotes weigh significantly more than wild-type males; as adults, mutant males are, on average, 40% heavier than wild-type males
• increased growth is also significant but less pronounced in females, though adult female homozygotes typically attain the weight of wild-type males
• increased body weight results from the proportionate enlargement of most visceral organs and is not attributed to accumulated fatty tissue
• sexually dimorphic or male-specific organs are not disproportionately enlarged
• carcass weight is also increased, indicating that muscle and bone may contribute to increased size
• male homozygotes display significantly a increased body length relative to wild-type males, although tail length is normal
• a similar but less pronounced trend is noted in the body length of female homozygotes
• homozygotes display accelerated growth after weaning i.e. beginning at around 3-4 weeks of age

limbs/digits/tail
• the mutant tibia is significantly longer than in wild-type controls

skeleton
• male homozygotes display significantly increased long bone lengths relative to wild-type males
• a similar but less pronounced trend is noted in the long bone lengths of female homozygotes
• however, bone architecture, including the epiphiseal growth plates of the femur and tibia, is histologically normal
• the mutant tibia is significantly longer than in wild-type controls

respiratory system
• at 2 months of age, 6 of 9 male, but only 3 of 10 female homozygotes show increased collagen deposition around the bronchi and vessels of the lungs; some alveolar sacs are occasionally involved

liver/biliary system
• at 2 months of age, a minority of both male and female homozygotes display excess collagen accumulation around occasional hepatic vessels and bile ducts

digestive/alimentary system
• at 2 months of age, a minority of both male and female homozygotes display excess collagen accumulation in duct tissue of the pancreas
• at 2 months of age, a minority of both male and female homozygotes display excess collagen accumulation in duct tissue of the salivary glands

endocrine/exocrine glands
• at 2 months of age, a minority of both male and female homozygotes display excess collagen accumulation in duct tissue of the pancreas
• at 2 months of age, a minority of both male and female homozygotes display excess collagen accumulation in duct tissue of the salivary glands

homeostasis/metabolism
• RNase protection assays indicate increased IGF-I production in several organs (heart, lungs and spleen), but not in liver, bone, fat or muscle
• however, no increase in serum IGF-I concentration is observed, consistent with normal production in the liver (major source of circulating IGF-I)
• at 6-7 weeks of age, all male and female homozygotes studied show decreased levels of major urinary protein (MUP) in their urine

renal/urinary system
• at 6-7 weeks of age, all male and female homozygotes studied show decreased levels of major urinary protein (MUP) in their urine

adipose tissue
N
• neither male nor female mutants accumulate significantly more abdominal fatty tissue than wild-type mice

integument
• adult homozygotes display a significantly thickened dermis, although most organs (including kidney, heart, spleen, thymus, lymph nodes, femur, sternum, gonads and bladder) appear histologically normal
• dermal thickening is associated with excessive collagen accumulation in all of male (7/7), and less prominently in female (6/8) homozygotes




Genotype
MGI:5431237
hm2
Allelic
Composition
Socs2tm1Wehi/Socs2tm1Wehi
Genetic
Background
involves: C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Socs2tm1Wehi mutation (0 available); any Socs2 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• in fasted mice fed a high fat diet
• in mice fed standard chow
• in mice fed standard chow or a high fat diet
• in mice fed standard chow or a high fat diet
• in mice fed a high fat diet
• in mice fed a high fat diet to a greater extent than in wild-type mice
• in mice fed a high fat diet to a greater extent than in wild-type mice
• mice fed a high fat diet exhibit less of an increased in liver triglyceride levels with increased hepatic triglyceride secretion compared with wild-type mice
• in the muscles of mice fed standard chow with a further increase in mice fed a high fat diet

muscle
• in the muscles of mice fed standard chow with a further increase in mice fed a high fat diet

liver/biliary system
• mice fed a high fat diet exhibit less of an increased in liver triglyceride levels with increased hepatic triglyceride secretion compared with wild-type mice
• as determined by expression of genes for inflammatory cytokines in mice fed a high fat diet
• when fed a high fat diet, mice develop a less extensive steatosis with a microvesicular pattern compared with macrovesicular steatosis in wild-type mice

adipose tissue
• in mice fed a high fat diet

immune system
• enhanced phagocytosis in bone marrow derived macrophage in response to LPS
• in mice fed standard chow or a high fat diet
• in mice fed standard chow or a high fat diet
• from bone marrow derived macrophage in response to LPS
• from bone marrow derived macrophage in response to LPS
• from bone marrow derived macrophage in response to LPS
• as determined by expression of genes for inflammatory cytokines in mice fed a high fat diet

hematopoietic system
• enhanced phagocytosis in bone marrow derived macrophage in response to LPS




Genotype
MGI:3808832
ht3
Allelic
Composition
Socs2tm1Wehi/Socs2+
Genetic
Background
C57BL/6-Socs2tm1Wehi
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Socs2tm1Wehi mutation (0 available); any Socs2 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• at 12 weeks of age, adult male heterozygotes show an intermediate body weight relative to wild-type and homozygous mutant littermates
• in contrast, female heterozygotes are not significantly heavier than wild-type females




Genotype
MGI:6507212
cx4
Allelic
Composition
Phf6tm1.2Avo/Y
Socs2tm1Wehi/Socs2tm1Wehi
Genetic
Background
involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Phf6tm1.2Avo mutation (0 available); any Phf6 mutation (12 available)
Socs2tm1Wehi mutation (0 available); any Socs2 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
N
• mice show partial rescue of the growth defects of hemizygous Phf6tm1.1Avo males, with an increase in body weight from 5 weeks of age, and no differences after 8 weeks





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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory