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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Shc1tm7Paw
targeted mutation 7, Tony Pawson
MGI:3716781
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Shc1tm7Paw/Shc1tm7Paw involves: 129S1/Sv * 129X1/SvJ MGI:3717094
ht2
Shc1tm3Paw/Shc1tm7Paw involves: 129S1/Sv * 129X1/SvJ MGI:3717108
cn3
Myl1tm1(cre)Sjb/Myl1+
Shc1tm7Paw/Shc1tm9Paw
involves: 129S1/Sv * 129X1/SvJ MGI:3717106
cx4
Shc1tm7Paw/Shc1+
Tg(MMTV-PyVT)634Mul/0
involves: 129S1/Sv * 129X1/SvJ * FVB/N MGI:4361926


Genotype
MGI:3717094
hm1
Allelic
Composition
Shc1tm7Paw/Shc1tm7Paw
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shc1tm7Paw mutation (0 available); any Shc1 mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype



Genotype
MGI:3717108
ht2
Allelic
Composition
Shc1tm3Paw/Shc1tm7Paw
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shc1tm3Paw mutation (0 available); any Shc1 mutation (66 available)
Shc1tm7Paw mutation (0 available); any Shc1 mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice display motor defects more severe than than transheterozygous Shc1tm3Paw/tm4Paw mice

nervous system
• between P22 and P35, muscle spindles are abnormal and numbers are 13% of controls
• intrafusal fiber numbers are 35.9% of control numbers

muscle
• between P22 and P35, muscle spindles are abnormal and numbers are 13% of controls
• intrafusal fiber numbers are 35.9% of control numbers




Genotype
MGI:3717106
cn3
Allelic
Composition
Myl1tm1(cre)Sjb/Myl1+
Shc1tm7Paw/Shc1tm9Paw
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myl1tm1(cre)Sjb mutation (2 available); any Myl1 mutation (17 available)
Shc1tm7Paw mutation (0 available); any Shc1 mutation (66 available)
Shc1tm9Paw mutation (0 available); any Shc1 mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• motor abnormalities are similar to those observed in Shc1tm7Paw homozygotes

muscle
• between P22 and P35, muscle spindle and intrafusal fiber numbers are reduced compared to controls

nervous system
• between P22 and P35, muscle spindle and intrafusal fiber numbers are reduced compared to controls




Genotype
MGI:4361926
cx4
Allelic
Composition
Shc1tm7Paw/Shc1+
Tg(MMTV-PyVT)634Mul/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shc1tm7Paw mutation (0 available); any Shc1 mutation (66 available)
Tg(MMTV-PyVT)634Mul mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• glands contain combination of tumor and hyperplastic structures
• combination of adenomas and cystic hyperplasias are seen in mammary glands
• tumor angiogenesis is decreased relative to tumors from Tg(MMTV-PyVT)634Mul single mutants
• number of mice displaying lung metastases is decreased compared to Tg(MMTV-PyVT)634Mul single mutants (60 vs 91 mice)
• mammary tumor latency is strongly increased compared to Tg(MMTV-PyVT)634Mul single mutants (95 days vs 66 days)

endocrine/exocrine glands
• glands contain combination of tumor and hyperplastic structures
• glands contain combination of tumor and hyperplastic structures
• combination of adenomas and cystic hyperplasias are seen in mammary glands
• tumor angiogenesis is decreased relative to tumors from Tg(MMTV-PyVT)634Mul single mutants

integument
• glands contain combination of tumor and hyperplastic structures
• glands contain combination of tumor and hyperplastic structures
• combination of adenomas and cystic hyperplasias are seen in mammary glands
• tumor angiogenesis is decreased relative to tumors from Tg(MMTV-PyVT)634Mul single mutants





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory