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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pdgfratm10(Pdgfra/tor)Sor
targeted mutation 10, Philippe Soriano
MGI:2663635
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Pdgfratm10(Pdgfra/tor)Sor/Pdgfratm10(Pdgfra/tor)Sor either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6) MGI:2663637
ht2
Pdgfratm10(Pdgfra/tor)Sor/Pdgfratm11(EGFP)Sor either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6) MGI:2663660


Genotype
MGI:2663637
hm1
Allelic
Composition
Pdgfratm10(Pdgfra/tor)Sor/Pdgfratm10(Pdgfra/tor)Sor
Genetic
Background
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfratm10(Pdgfra/tor)Sor mutation (0 available); any Pdgfra mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most mutant embryos die by E15.5 but a small percentage (9%) survive to E18.5

cardiovascular system
N
• angiogenesis is normal and hemorrhaging is rarely present
• mutants exhibiting severe facial clefting show incomplete septa formation; mutants with little facial clefting do not display septation defects

craniofacial
• late-stage fetuses display a cleft face or palate
• 10% of mutant embryos exhibit severe facial clefting, but remaining mutants display lesser degree of facial clefting compared to Pdgfra-null mutants

skeleton
• ribs do not fuse at the midline and thus do not form the sternum
• failure of ribs to fuse at the midline

nervous system
• late-stage fetuses show failed ventral closure
• late-stage fetuses show failed ventral closure and spina bifida, although defects are less severe than in Pdgfra null mice

homeostasis/metabolism
• edema is detected only in very-late stage (E17) mutants

digestive/alimentary system
• late-stage fetuses display a cleft face or palate

embryo
• late-stage fetuses show failed ventral closure
• late-stage fetuses show failed ventral closure and spina bifida, although defects are less severe than in Pdgfra null mice

growth/size/body
• late-stage fetuses display a cleft face or palate
• 10% of mutant embryos exhibit severe facial clefting, but remaining mutants display lesser degree of facial clefting compared to Pdgfra-null mutants




Genotype
MGI:2663660
ht2
Allelic
Composition
Pdgfratm10(Pdgfra/tor)Sor/Pdgfratm11(EGFP)Sor
Genetic
Background
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfratm10(Pdgfra/tor)Sor mutation (0 available); any Pdgfra mutation (88 available)
Pdgfratm11(EGFP)Sor mutation (1 available); any Pdgfra mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
• the epithelial cell layer between the chorioallantoic plate and labyrinth is completely absent





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory