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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Polr1aem1Knwea
endonuclease-mediated mutation 1, Kathryn Nicole Weaver
MGI:7526140
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Polr1aem1Knwea/Polr1aem1Knwea C57BL/6-Polr1aem1Knwea MGI:7526443
ht2
Polr1aem1Knwea/Polr1a+ C57BL/6-Polr1aem1Knwea MGI:7526438
cn3
Foxg1tm1.1(cre)Ddmo/0
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
Polr1aem1Knwea/Polr1atm1c(EUCOMM)Hmgu
involves: 129S1/Sv * 129T/Sv * 129X1/SvJ * C57BL/6N MGI:7526484
cn4
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
Polr1aem1Knwea/Polr1atm1c(EUCOMM)Hmgu
Tg(Wnt1-cre/Esr1*)10Rth/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6N MGI:7526471
cn5
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
Polr1aem1Knwea/Polr1atm1c(EUCOMM)Hmgu
Tg(Sox10-cre)1Wdr/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6N * CBA MGI:7526470


Genotype
MGI:7526443
hm1
Allelic
Composition
Polr1aem1Knwea/Polr1aem1Knwea
Genetic
Background
C57BL/6-Polr1aem1Knwea
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Polr1aem1Knwea mutation (0 available); any Polr1a mutation (93 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:7526438
ht2
Allelic
Composition
Polr1aem1Knwea/Polr1a+
Genetic
Background
C57BL/6-Polr1aem1Knwea
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Polr1aem1Knwea mutation (0 available); any Polr1a mutation (93 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
N
• mice born at expected Mendelian ratios and normal sex ratio

growth/size/body
N
• no obvious phenotype

reproductive system




Genotype
MGI:7526484
cn3
Allelic
Composition
Foxg1tm1.1(cre)Ddmo/0
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
Polr1aem1Knwea/Polr1atm1c(EUCOMM)Hmgu
Genetic
Background
involves: 129S1/Sv * 129T/Sv * 129X1/SvJ * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxg1tm1.1(cre)Ddmo mutation (1 available); any Foxg1 mutation (28 available)
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo mutation (10 available); any Gt(ROSA)26Sor mutation (944 available)
Polr1aem1Knwea mutation (0 available); any Polr1a mutation (93 available)
Polr1atm1c(EUCOMM)Hmgu mutation (0 available); any Polr1a mutation (93 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• in E14 and E17 embryos
• normal in E12 embryos




Genotype
MGI:7526471
cn4
Allelic
Composition
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
Polr1aem1Knwea/Polr1atm1c(EUCOMM)Hmgu
Tg(Wnt1-cre/Esr1*)10Rth/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo mutation (10 available); any Gt(ROSA)26Sor mutation (944 available)
Polr1aem1Knwea mutation (0 available); any Polr1a mutation (93 available)
Polr1atm1c(EUCOMM)Hmgu mutation (0 available); any Polr1a mutation (93 available)
Tg(Wnt1-cre/Esr1*)10Rth mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

craniofacial
• starting in E9.5 embryos, worsening with age

growth/size/body
• starting in E9.5 embryos, worsening with age

cardiovascular system
N
• normal outflow tract septation in E12 embryos




Genotype
MGI:7526470
cn5
Allelic
Composition
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
Polr1aem1Knwea/Polr1atm1c(EUCOMM)Hmgu
Tg(Sox10-cre)1Wdr/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6N * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo mutation (10 available); any Gt(ROSA)26Sor mutation (944 available)
Polr1aem1Knwea mutation (0 available); any Polr1a mutation (93 available)
Polr1atm1c(EUCOMM)Hmgu mutation (0 available); any Polr1a mutation (93 available)
Tg(Sox10-cre)1Wdr mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• median lip notches in some E14-E15 embryos
• in some E14-E15 embryos
• in some E14-E15 embryos

digestive/alimentary system
• in some E14-E15 embryos

growth/size/body
• median lip notches in some E14-E15 embryos
• in some E14-E15 embryos
• in some E14-E15 embryos





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory