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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tagln+
wild type
MGI:2440350
Summary 9 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Pdcd10tm1Wami/Pdcd10tm1Wami
Taglntm2(cre)Yec/Tagln+
involves: 129 * 129S6/SvEvTac * C57BL/6 MGI:5002666
cn2
Msx1tm1Bero/Msx1tm1Bero
Msx2tm1Bero/Msx2tm1Yvla
Taglntm2(cre)Yec/Tagln+
involves: 129P2/OlaHsd * 129S2/SvPas * 129S6/SvEvTac * NMRI MGI:5297709
cn3
Apoetm1Unc/Apoetm1Unc
Ddit3tm1.1Irt/Ddit3tm1.1Irt
Taglntm2(cre)Yec/Tagln+
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J MGI:5781094
cn4
Msx1tm1Rem/Msx1tm1Rem
Msx2tm1Yvla/Msx2tm1Yvla
Taglntm2(cre)Yec/Tagln+
involves: 129S2/SvPas * 129S6/SvEvTac * NMRI MGI:5297710
cn5
Stk11tm1.1Rdp/Stk11+
Taglntm1(cre/ERT2)Feil/Tagln+
involves: 129S/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL MGI:3814821
cn6
Stk11tm1.1Rdp/Stk11tm1.1Rdp
Taglntm1(cre/ERT2)Feil/Tagln+
involves: 129S/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL MGI:3814824
cx7
Taglntm1Liw/Tagln+
Tbx18tm1.1Mwmy/Tbx18tm1.1Mwmy
involves: 129 * C57BL/6J MGI:5553118
cx8
Prkg1tm2.1Naw/Prkg1tm2.1Naw
Taglntm1(PRKG1*)Hfm/Tagln+
involves: 129S1/Sv * 129X1/SvJ MGI:3797264
cx9
Prkg1tm2.1Naw/Prkg1tm2.1Naw
Taglntm2(PRKG1*)Hfm/Tagln+
involves: 129S1/Sv * 129X1/SvJ MGI:3797265


Genotype
MGI:5002666
cn1
Allelic
Composition
Pdcd10tm1Wami/Pdcd10tm1Wami
Taglntm2(cre)Yec/Tagln+
Genetic
Background
involves: 129 * 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdcd10tm1Wami mutation (0 available); any Pdcd10 mutation (18 available)
Taglntm2(cre)Yec mutation (1 available); any Tagln mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• mice exhibit normal Mendelian ratio after weaning

cardiovascular system
N
• mice exhibit normal retinal vascular development




Genotype
MGI:5297709
cn2
Allelic
Composition
Msx1tm1Bero/Msx1tm1Bero
Msx2tm1Bero/Msx2tm1Yvla
Taglntm2(cre)Yec/Tagln+
Genetic
Background
involves: 129P2/OlaHsd * 129S2/SvPas * 129S6/SvEvTac * NMRI
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Msx1tm1Bero mutation (1 available); any Msx1 mutation (18 available)
Msx2tm1Bero mutation (1 available); any Msx2 mutation (23 available)
Msx2tm1Yvla mutation (0 available); any Msx2 mutation (23 available)
Taglntm2(cre)Yec mutation (1 available); any Tagln mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• superficial temporal artery is more branched than in controls
• at E11.5, carotid artery (CA) overbranching is observed
• vertebral artery (VA) caliber is increased relative to controls
• number of smooth muscle actin-positive cells in CA is half that observed in controls
• in the head, aneurysms are frequently observed
• in the head, hemorrhages are frequently observed

muscle
• number of smooth muscle actin-positive cells in CA is half that observed in controls

nervous system
• in the head, hemorrhages are frequently observed




Genotype
MGI:5781094
cn3
Allelic
Composition
Apoetm1Unc/Apoetm1Unc
Ddit3tm1.1Irt/Ddit3tm1.1Irt
Taglntm2(cre)Yec/Tagln+
Genetic
Background
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apoetm1Unc mutation (33 available); any Apoe mutation (146 available)
Ddit3tm1.1Irt mutation (1 available); any Ddit3 mutation (20 available)
Taglntm2(cre)Yec mutation (1 available); any Tagln mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• aortic root shows a approximate 30% reduction in lesion area and necrotic area compared to Apoetm1Unc Ddit3tm1.1Irt double homozygotes, indicating decreased atherosclerotic plaque progression
• smooth muscle cell content is lower in aortic arch lesions compared to Ddit3tm1.1Irt Apoetm1Unc double homozygotes
• mice on a Western diet show a lower content of alpha-actin-positive vascular smooth muscle cells in the lesions compared to Ddit3tm1.1Irt Apoetm1Unc double homozygotes
• lesions show decreased vascular smooth muscle cell proliferation

homeostasis/metabolism
N
• after 12 weeks of Western diet feeding, mice exhibit similar body weight, blood glucose, total plasma cholesterol, HDL cholesterol, plasma triglycerides, and blood pressure as Apoetm1Unc Ddit3tm1.1Irt double homozygotes




Genotype
MGI:5297710
cn4
Allelic
Composition
Msx1tm1Rem/Msx1tm1Rem
Msx2tm1Yvla/Msx2tm1Yvla
Taglntm2(cre)Yec/Tagln+
Genetic
Background
involves: 129S2/SvPas * 129S6/SvEvTac * NMRI
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Msx1tm1Rem mutation (1 available); any Msx1 mutation (18 available)
Msx2tm1Yvla mutation (0 available); any Msx2 mutation (23 available)
Taglntm2(cre)Yec mutation (1 available); any Tagln mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• increased carotid artery section surface (increased vessel diameter) is observed
• a reduction in vascular smooth muscle cell (VSMC) coverage (depletion of mural cells) is observed

muscle
• a reduction in vascular smooth muscle cell (VSMC) coverage (depletion of mural cells) is observed




Genotype
MGI:3814821
cn5
Allelic
Composition
Stk11tm1.1Rdp/Stk11+
Taglntm1(cre/ERT2)Feil/Tagln+
Genetic
Background
involves: 129S/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Stk11tm1.1Rdp mutation (0 available); any Stk11 mutation (34 available)
Taglntm1(cre/ERT2)Feil mutation (0 available); any Tagln mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• almost 50% of tamoxifen-treated animals die by 18 months from gastrointestinal obstruction (average lifespan 13.5 months); widespread gastrointestinal polyposis is found at time of necropsy

digestive/alimentary system
N
• with 2 intraperitoneal injections of tamoxifen at 6 weeks of age, no abnormalities are seen at 3 and 8 months of age
• at 11 months, gastrointestinal tract polyps are observed in <60% of tamoxifen-treated animals
• average polyp size is smaller than in Stk11tm1.2Rdp/+ mice at 11 months
• tumor formation (polyposis) in the gastrointestinal tract is increased greatly relative to controls
• tumors are characterized by a smooth muscle core, abundant stroma and hyperplastic epithelia without dysplasia
• at 11 months, mice present with severe gastrointestinal obstruction

neoplasm
• tumor formation (polyposis) in the gastrointestinal tract is increased greatly relative to controls
• tumors are characterized by a smooth muscle core, abundant stroma and hyperplastic epithelia without dysplasia




Genotype
MGI:3814824
cn6
Allelic
Composition
Stk11tm1.1Rdp/Stk11tm1.1Rdp
Taglntm1(cre/ERT2)Feil/Tagln+
Genetic
Background
involves: 129S/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Stk11tm1.1Rdp mutation (0 available); any Stk11 mutation (34 available)
Taglntm1(cre/ERT2)Feil mutation (0 available); any Tagln mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
digestive/alimentary system
• 75% of tamoxifen-treated animals develop gastrointestinal polyposis by 11 months
• average size of polyps is comparable to that seen in double heterozygotes
• tumor formation (polyposis) in the gastrointestinal tract is increased greatly relative to controls

neoplasm
• tumor formation (polyposis) in the gastrointestinal tract is increased greatly relative to controls




Genotype
MGI:5553118
cx7
Allelic
Composition
Taglntm1Liw/Tagln+
Tbx18tm1.1Mwmy/Tbx18tm1.1Mwmy
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Taglntm1Liw mutation (1 available); any Tagln mutation (26 available)
Tbx18tm1.1Mwmy mutation (0 available); any Tbx18 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• reduced smooth muscle content and shorter overall smooth muscle coverage at birth
• less developed branching network of subepicardial conduit vessels
• reduced smooth muscle content and shorter overall smooth muscle coverage at birth
• reduced overall diameter of the coronary stems and reduced branching index

muscle
• reduced smooth muscle content and shorter overall smooth muscle coverage at birth




Genotype
MGI:3797264
cx8
Allelic
Composition
Prkg1tm2.1Naw/Prkg1tm2.1Naw
Taglntm1(PRKG1*)Hfm/Tagln+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prkg1tm2.1Naw mutation (0 available); any Prkg1 mutation (59 available)
Taglntm1(PRKG1*)Hfm mutation (0 available); any Tagln mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice have a median survival time of 52 weeks
• this survival time is significantly longer than Prkg1tm2.1Naw homozygote that do not carry the knock-in allele

reproductive system
• female mice have a reduced success rate of pregnancy
• mice have slightly reduced litter size of 3 to 6 pups




Genotype
MGI:3797265
cx9
Allelic
Composition
Prkg1tm2.1Naw/Prkg1tm2.1Naw
Taglntm2(PRKG1*)Hfm/Tagln+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prkg1tm2.1Naw mutation (0 available); any Prkg1 mutation (59 available)
Taglntm2(PRKG1*)Hfm mutation (0 available); any Tagln mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice have a median survival time of 52 weeks
• this survival time is significantly longer than Prkg1tm2.1Naw homozygote that do not carry the knock-in allele

reproductive system
• female mice have a reduced success rate of pregnancy
• mice have slightly reduced litter size of 3 to 6 pups





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last database update
06/12/2024
MGI 6.13
The Jackson Laboratory