About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Pdgfra-cre)1Clc
transgene insertion 1, Constance L Cepko
MGI:4837746
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Senp1tm1Wami/Senp1tm1Wami
Tg(Pdgfra-cre)1Clc/0
B6.Cg-Senp1tm1Wami Tg(Pdgfra-cre)1Clc MGI:5707772
cn2
Crb2tm1.1Wij/Crb2tm1.1Wij
Tg(Pdgfra-cre)1Clc/0
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J MGI:5586709
cn3
Igs1tm11(CAG-Bgeo,-Edn2)Nat/Igs1+
Tg(Pdgfra-cre)1Clc/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5544087
cn4
Bbs1tm2Vcs/Bbs1tm2Vcs
Tg(Pdgfra-cre)1Clc/0
involves: 129S6/SvEvTac * C57BL/6 MGI:5474570
cn5
Acvr1tm1Glh/Acvr1+
Gt(ROSA)26Sortm1.2(CAG-EGFP)Glh/Gt(ROSA)26Sor+
Tg(Pdgfra-cre)1Clc/0
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * FVB/N MGI:7278773
cn6
Ephx2tm1.1Arte/Ephx2tm1.1Arte
Tg(Pdgfra-cre)1Clc/0
involves: C57BL/6 MGI:5609318


Genotype
MGI:5707772
cn1
Allelic
Composition
Senp1tm1Wami/Senp1tm1Wami
Tg(Pdgfra-cre)1Clc/0
Genetic
Background
B6.Cg-Senp1tm1Wami Tg(Pdgfra-cre)1Clc
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Senp1tm1Wami mutation (0 available); any Senp1 mutation (65 available)
Tg(Pdgfra-cre)1Clc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• age-dependent increase in glucose levels, with an early onset of diabetes at 6 weeks of age
• increase in glucose levels is seen with or without fasting

growth/size/body
• lower body weight after onset of diabetes

endocrine/exocrine glands
• increase in apoptosis of beta cells
• structures of pancreatic islets are disrupted, with increased apoptosis of beta cells after onset of diabetes and more severe at later stages
• increase in apoptosis of beta cells after onset of diabetes and more severe at later stages

cellular
• increase in apoptosis of beta cells




Genotype
MGI:5586709
cn2
Allelic
Composition
Crb2tm1.1Wij/Crb2tm1.1Wij
Tg(Pdgfra-cre)1Clc/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Crb2tm1.1Wij mutation (0 available); any Crb2 mutation (52 available)
Tg(Pdgfra-cre)1Clc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice are born at a 5-fold reduced ratio than expected

vision/eye
• protrusion of photoreceptor nuclei into the subretinal space at sites of outer limiting membrane disruption at 5 months of age
• however, 5 month old mice show normal electroretinography (ERG), scanning laser ophthalmoscopy, and spectral domain optical coherence tomography readings
• ectopic Muller glial cell nuclei in the outer nuclear layer and activated Muller glial cells are seen at 5 months of age
• at 5 months of age, a reduction of the outer nuclear layer thickness is seen
• disruptions of the outer limiting membrane at the periphery of the retina, where rows of photoreceptor nuclei protrude into the subretinal space, are seen at 1, 3, and 5 months of age




Genotype
MGI:5544087
cn3
Allelic
Composition
Igs1tm11(CAG-Bgeo,-Edn2)Nat/Igs1+
Tg(Pdgfra-cre)1Clc/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Igs1tm11(CAG-Bgeo,-Edn2)Nat mutation (1 available); any Igs1 mutation (10 available)
Tg(Pdgfra-cre)1Clc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Interstitial tip cells in adult Igs1tm11(CAG-Bgeo,-Edn2)Nat/Igs1+ Tg(Pdgfra-cre)1Clc/0 retinas

vision/eye
• intraretinal capillaries are larger and more numerous; however a large number of these terminate with blind endings
• blind endings are most numerous in the inner plexiform layer and are typically decorated with multiple filopodia

cardiovascular system
• intraretinal capillaries are larger and more numerous; however a large number of these terminate with blind endings
• blind endings are most numerous in the inner plexiform layer and are typically decorated with multiple filopodia




Genotype
MGI:5474570
cn4
Allelic
Composition
Bbs1tm2Vcs/Bbs1tm2Vcs
Tg(Pdgfra-cre)1Clc/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bbs1tm2Vcs mutation (0 available); any Bbs1 mutation (70 available)
Tg(Pdgfra-cre)1Clc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• motile cilia in the lateral ventricles are normal
• non-obstructive beginning at P3

cellular

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Bardet-Biedl syndrome 1 DOID:0110123 OMIM:209900
J:194096




Genotype
MGI:7278773
cn5
Allelic
Composition
Acvr1tm1Glh/Acvr1+
Gt(ROSA)26Sortm1.2(CAG-EGFP)Glh/Gt(ROSA)26Sor+
Tg(Pdgfra-cre)1Clc/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Acvr1tm1Glh mutation (0 available); any Acvr1 mutation (44 available)
Gt(ROSA)26Sortm1.2(CAG-EGFP)Glh mutation (0 available); any Gt(ROSA)26Sor mutation (942 available)
Tg(Pdgfra-cre)1Clc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• skeletal muscle exhibits pinch injury-induced heterotopic ossification

skeleton
• spontaneous heterotopic ossification is seen infrequently in some 2-week-old mice and is present in all 4-week-old mice and extensive in all surviving mice by 6 weeks of age
• heterotopic ossification is seen in the musculature, tendons, and ligaments at diverse locations
• skeletal elements resulting from spontaneous heterotopic ossification are derived almost exclusively from recombined cells
• all mice treated with an anti-activin A mAb prior to onset of heterotopic ossification for 4 weeks survive to 6 weeks of age and 8 of 9 mice show no evidence of heterotopic ossification and no spontaneous heterotopic ossification is not seen in treated 16-week-old mice

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
fibrodysplasia ossificans progressiva DOID:13374 OMIM:135100
J:257905




Genotype
MGI:5609318
cn6
Allelic
Composition
Ephx2tm1.1Arte/Ephx2tm1.1Arte
Tg(Pdgfra-cre)1Clc/0
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ephx2tm1.1Arte mutation (0 available); any Ephx2 mutation (39 available)
Tg(Pdgfra-cre)1Clc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• significant delay in the radial extension of the vascular plexus from the optic nerve to the periphery and decrease in the number of tip cells and filopodia
• significant delay in the radial extension of the vascular plexus from the optic nerve to the periphery and decrease in the number of tip cells and filopodia

vision/eye
• significant delay in the radial extension of the vascular plexus from the optic nerve to the periphery and decrease in the number of tip cells and filopodia





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