About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rasgrf1tm4.1Pds
targeted mutation 4.1, Paul D Soloway
MGI:3611767
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Rasgrf1tm4.1Pds/Rasgrf1+ involves: 129S4/SvJaeSor * C57BL/6 MGI:3620519
cn2
Meox2tm1(cre)Sor/Meox2+
Rasgrf1tm4.1Pds/Rasgrf1+
involves: 129S4/SvJaeSor * C57BL/6 MGI:3698139
cn3
Rasgrf1tm4.1Pds/Rasgrf1+
Tg(Zp3-cre)3Mrt/0
involves: 129S4/SvJaeSor * C57BL/6 * FVB/N MGI:3698138
cn4
Rasgrf1tm4.1Pds/Rasgrf1+
Tg(Nes-cre)1Kln/0
involves: 129S4/SvJaeSor * C57BL/6 * SJL MGI:3698137


Genotype
MGI:3620519
ht1
Allelic
Composition
Rasgrf1tm4.1Pds/Rasgrf1+
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rasgrf1tm4.1Pds mutation (0 available); any Rasgrf1 mutation (65 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• DNA methylation of and Rasgrf1 expression from floxed allele are unaffected




Genotype
MGI:3698139
cn2
Allelic
Composition
Meox2tm1(cre)Sor/Meox2+
Rasgrf1tm4.1Pds/Rasgrf1+
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Meox2tm1(cre)Sor mutation (3 available); any Meox2 mutation (18 available)
Rasgrf1tm4.1Pds mutation (0 available); any Rasgrf1 mutation (65 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
N
• loss of paternal repeats does not affect expression of Rasgrf1 in neonatal brain
• loss of paternal repeats at E5.5 in the epiblast does not result in changes to methylation state of the paternal allele, in contrast with deletion earlier in development




Genotype
MGI:3698138
cn3
Allelic
Composition
Rasgrf1tm4.1Pds/Rasgrf1+
Tg(Zp3-cre)3Mrt/0
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rasgrf1tm4.1Pds mutation (0 available); any Rasgrf1 mutation (65 available)
Tg(Zp3-cre)3Mrt mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• Rasgrf1 expression from paternal allele is silenced in neonatal brain
• DNA from progeny has lost almost all differentially methylated domain (DMD) methylation from the paternal allele
• methylation on floxed allele cannot be maintained upon cre-mediated recombination in zygote




Genotype
MGI:3698137
cn4
Allelic
Composition
Rasgrf1tm4.1Pds/Rasgrf1+
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rasgrf1tm4.1Pds mutation (0 available); any Rasgrf1 mutation (65 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
N
• loss of paternal repeats does not affect expression of Rasgrf1 in neonatal brain
• loss of paternal repeats at E11 in the central nervous system does not result in changes to methylation state of the paternal allele, in contrast with deletion earlier in development





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
04/23/2024
MGI 6.23
The Jackson Laboratory