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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Sec24ctm1c(EUCOMM)Wtsi
targeted mutation 1c, Wellcome Trust Sanger Institute
MGI:5501469
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ptf1atm1.1(cre)Cvw/Ptf1a+
Sec24ctm1c(EUCOMM)Wtsi/Sec24ctm1c(EUCOMM)Wtsi
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:5896386
cn2
Meox2tm1(cre)Sor/Meox2+
Sec24ctm1c(EUCOMM)Wtsi/Sec24ctm1c(EUCOMM)Wtsi
involves: 129S4/SvJaeSor * C57BL/6 * SJL MGI:5896387
cn3
Sec24ctm1c(EUCOMM)Wtsi/Sec24ctm1c(EUCOMM)Wtsi
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
involves: C57BL/6 * DBA * SJL MGI:5896384
cn4
Sec24ctm1c(EUCOMM)Wtsi/Sec24ctm1c(EUCOMM)Wtsi
Tg(Vil1-cre)997Gum/0
involves: C57BL/6 * SJL MGI:5896385
cn5
Sec24ctm1c(EUCOMM)Wtsi/Sec24ctm1c(EUCOMM)Wtsi
Tg(Tagln-cre)1Her/0
involves: C57BL/6 * SJL MGI:5896388


Genotype
MGI:5896386
cn1
Allelic
Composition
Ptf1atm1.1(cre)Cvw/Ptf1a+
Sec24ctm1c(EUCOMM)Wtsi/Sec24ctm1c(EUCOMM)Wtsi
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptf1atm1.1(cre)Cvw mutation (1 available); any Ptf1a mutation (30 available)
Sec24ctm1c(EUCOMM)Wtsi mutation (1 available); any Sec24c mutation (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
N
• no defects in pancreas morphology are detected

growth/size/body
N
• no abnormalities in growth or weight gain are detected on either a normal chow or high fat diet compared to diet-matched controls

homeostasis/metabolism
N
• no differences in plasma cholesterol, triglyceride or insulin levels




Genotype
MGI:5896387
cn2
Allelic
Composition
Meox2tm1(cre)Sor/Meox2+
Sec24ctm1c(EUCOMM)Wtsi/Sec24ctm1c(EUCOMM)Wtsi
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Meox2tm1(cre)Sor mutation (3 available); any Meox2 mutation (18 available)
Sec24ctm1c(EUCOMM)Wtsi mutation (1 available); any Sec24c mutation (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all die before 2 weeks of age




Genotype
MGI:5896384
cn3
Allelic
Composition
Sec24ctm1c(EUCOMM)Wtsi/Sec24ctm1c(EUCOMM)Wtsi
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
Genetic
Background
involves: C57BL/6 * DBA * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sec24ctm1c(EUCOMM)Wtsi mutation (1 available); any Sec24c mutation (39 available)
Speer6-ps1Tg(Alb-cre)21Mgn mutation (6 available); any Speer6-ps1 mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
N
• no abnormalities in growth or weight gain are detected on either a normal chow or high fat diet compared to diet-matched controls

homeostasis/metabolism
N
• no differences in plasma cholesterol or triglyceride levels




Genotype
MGI:5896385
cn4
Allelic
Composition
Sec24ctm1c(EUCOMM)Wtsi/Sec24ctm1c(EUCOMM)Wtsi
Tg(Vil1-cre)997Gum/0
Genetic
Background
involves: C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sec24ctm1c(EUCOMM)Wtsi mutation (1 available); any Sec24c mutation (39 available)
Tg(Vil1-cre)997Gum mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
N
• no abnormalities in growth or weight gain are detected on either a normal chow or high fat diet compared to diet-matched controls

homeostasis/metabolism
N
• no differences in plasma cholesterol or triglyceride levels




Genotype
MGI:5896388
cn5
Allelic
Composition
Sec24ctm1c(EUCOMM)Wtsi/Sec24ctm1c(EUCOMM)Wtsi
Tg(Tagln-cre)1Her/0
Genetic
Background
involves: C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sec24ctm1c(EUCOMM)Wtsi mutation (1 available); any Sec24c mutation (39 available)
Tg(Tagln-cre)1Her mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• viable and fertile





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory