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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pdgfratm1Sor
targeted mutation 1, Philippe Soriano
MGI:1926714
Summary 9 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Pdgfratm1Sor/Pdgfratm1Sor either: 129S4/SvJaeSor-Pdgfratm1Sor or (involves: 129S4/SvJaeSor * C57BL/6J) MGI:2175214
hm2
Pdgfratm1Sor/Pdgfratm1Sor involves: 129S4/SvJaeSor MGI:3838620
ht3
Pdgfratm1Sor/Pdgfra+ either: 129S4/SvJaeSor-Pdgfratm1Sor or (involves: 129S4/SvJaeSor * C57BL/6J) MGI:3655071
ht4
Pdgfratm1Sor/Pdgfratm7Sor either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6J) MGI:3694556
cx5
Pdgfratm1Sor/Pdgfra+
Plekha1Gt(ROSA)82Sor/Plekha1Gt(ROSA)82Sor
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6) MGI:3822917
cx6
Pdgfratm1Sor/Pdgfra+
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6) MGI:3823001
cx7
Pdgfratm1Sor/Pdgfra+
Sgpl1Gt(ROSA)78Sor/Sgpl1Gt(ROSA)78Sor
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6) MGI:3823017
cx8
Pdgfratm1Sor/Pdgfra+
Schip1Gt(ROSA)77Sor/Schip1Gt(ROSA)77Sor
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6) MGI:3823020
cx9
2610005L07RikGt(ROSA)73Sor/2610005L07RikGt(ROSA)73Sor
Pdgfratm1Sor/Pdgfra+
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6) MGI:3823024


Genotype
MGI:2175214
hm1
Allelic
Composition
Pdgfratm1Sor/Pdgfratm1Sor
Genetic
Background
either: 129S4/SvJaeSor-Pdgfratm1Sor or (involves: 129S4/SvJaeSor * C57BL/6J)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfratm1Sor mutation (0 available); any Pdgfra mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• several homozygotes are dead at E14 while survivors appear distended and hemorrhagic
• most homozygotes die by E16; survivors show extensive bleeding in the head and along the vertebral column which appears enlarged

nervous system
• at E15.5, the mutant neural tube is dorsally thinned and lacks a roof plate
• homozygotes exhibit defects in cranial neural crest cell development
• in thoracic vertebrae, and to a lesser extent in cervical vertebrae, neural arches fail to form a convex structure, resulting in spina bifida
• at E8 and E9, most mutant embryos display a very wavy neural tube
• at E10, >50% of mutant embryos have a very wavy neural tube

embryo
• at E9, a few mutant embryos exhibit defective yolk sac vasculature
• at E8, five of 6 homozygotes have not turned; ~25% and 50% of mutant embryos remain unturned at E9 and E10, respectively
• at E8, one of 6 homozygotes is severely retarded at the headfold stage
• at E9, 25% of mutant embryos are smaller than wild-type embryos
• at E10, 25% of mutant embryos are very small while another 25% appear normal
• at E11, >50% of mutant embryos appear normal while the remainder are smaller and exhibit a wavy neural tube
• at E15.5, the mutant neural tube is dorsally thinned and lacks a roof plate
• homozygotes exhibit defects in cranial neural crest cell development
• in thoracic vertebrae, and to a lesser extent in cervical vertebrae, neural arches fail to form a convex structure, resulting in spina bifida
• at E8 and E9, most mutant embryos display a very wavy neural tube
• at E10, >50% of mutant embryos have a very wavy neural tube

cardiovascular system
• at E9, a few mutant embryos exhibit defective yolk sac vasculature
• at E10, 25% of mutant embryos show pericardial edema
• at E9, a few mutant embryos show blood-filled blebs along the neural tube and head
• at E8, 2 of 6 mutant embryos show 2-4 subepidermal blebs flanking the neural tube
• at E14, surviving mutant embryos display bleeding at various locations
• by E16, survivors exhibit extensive bleeding in the head and along the vertebral column
• despite bleeding, septation in the heart proceeds normally in at least some of E15 survivors

homeostasis/metabolism
• at E12, mutant embryos show blebbing in multiple locations and edema, which increases in severity by E13
• at E10, 25% of mutant embryos show pericardial edema
• at E15.5, mutant embryos exhibit distended, edematous skin

growth/size/body
• at E13-E15, the nasal bone fails to fuse in the midline
• at E12, mutant embryos show a cleft face
• at E8, one of 6 homozygotes is severely retarded at the headfold stage
• at E9, 25% of mutant embryos are smaller than wild-type embryos
• at E10, 25% of mutant embryos are very small while another 25% appear normal
• at E11, >50% of mutant embryos appear normal while the remainder are smaller and exhibit a wavy neural tube
• at E15.5, tissues such as the liver are bulging from the abdominal wall musculature

craniofacial
• at E15, the mutant basisphenoid and temporal bones display retarded ossification
• in contrast, the basioccipital bone and the maxilla appear normal
• at E13-E15, the frontal bone shows incomplete fusion towards the top of the skull
• at E13-E15, the parietal bone shows incomplete fusion towards the top of the skull
• at E13-E15, the nasal bone fails to fuse in the midline
• at E13-E15, the zygomatic bone is absent
• at E12, mutant embryos show a cleft face

skeleton
• at E15, the mutant basisphenoid and temporal bones display retarded ossification
• in contrast, the basioccipital bone and the maxilla appear normal
• at E13-E15, the frontal bone shows incomplete fusion towards the top of the skull
• at E13-E15, the parietal bone shows incomplete fusion towards the top of the skull
• at E13-E15, the nasal bone fails to fuse in the midline
• at E13-E15, the zygomatic bone is absent
• at E15.5, mutant embryos display a poorly developed acromion
• at E15.5, most ribs are attached to sternal bands; however, mutant sternal bands are shorter, highly abnormal and fail to fuse
• at E15.5, almost all homozygotes display asymmetric rib bifurcations of a variable extent; first evident at E13
• at E15.5, almost all homozygotes display asymmetric rib fusions of a variable extent; first evident at E13
• at E15.5, mutant thoracic vertebrae show absence of flexure
• sacral and caudal vertebrae are slightly retarded in development but otherwise normal
• at E15.5, mutant embryos display severe arching of the spinal column
• at E15.5, mutant cervical vertebrae show extensive structural changes and anterior-posterior fusions of the arches, involving up to 4 cervical vertebrae in some cases
• in addition, the apposition of vertebrae at the level of the vertebral bodies is abnormal and bilaterally asymmetric

muscle
• at E10.5, mutant embryos show disorganized myotomal development, esp. at the level of more rostral somites
• at E10.5, mutant myotomes at the level of 15-20 most rostral somites are elongated instead of round, and missing or fused with adjacent myotomes
• in contrast, myotomal morphology appears normal in caudal somites

cellular
• at E10, mutant embryos show increased apoptosis in the somites, cephalic region and branchial arches i.e. on pathways followed by migrating cranial NCCs

pigmentation
N
• at E10-E13, homozygotes display no pigmentation defects with normal melanocyte migration/number around the ear and tail

integument
• at E15.5, mutant embryos exhibit distended, edematous skin
• at E15.5, mutant embryos show a very thin epidermal layer, that is separated from any dermal layer when blebbed
• at E12, mutant embryos show large blebs on their heads accompanied by bleeding

respiratory system
• at E13-E15, the nasal bone fails to fuse in the midline




Genotype
MGI:3838620
hm2
Allelic
Composition
Pdgfratm1Sor/Pdgfratm1Sor
Genetic
Background
involves: 129S4/SvJaeSor
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfratm1Sor mutation (0 available); any Pdgfra mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• slightly smaller than normal




Genotype
MGI:3655071
ht3
Allelic
Composition
Pdgfratm1Sor/Pdgfra+
Genetic
Background
either: 129S4/SvJaeSor-Pdgfratm1Sor or (involves: 129S4/SvJaeSor * C57BL/6J)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfratm1Sor mutation (0 available); any Pdgfra mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
N
• heterozygotes display absence of a pigmentation defect, indicating normal melanocyte migration




Genotype
MGI:3694556
ht4
Allelic
Composition
Pdgfratm1Sor/Pdgfratm7Sor
Genetic
Background
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6J)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfratm1Sor mutation (0 available); any Pdgfra mutation (88 available)
Pdgfratm7Sor mutation (0 available); any Pdgfra mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
N
• do not exhibit facial clefting

skeleton
• display skeletal abnormalities very similar to those seen in Pdgfratm5Sor homozygotes, however no data is presented in J:73817

integument
• exhibit blebbing along the midline of the head




Genotype
MGI:3822917
cx5
Allelic
Composition
Pdgfratm1Sor/Pdgfra+
Plekha1Gt(ROSA)82Sor/Plekha1Gt(ROSA)82Sor
Genetic
Background
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfratm1Sor mutation (0 available); any Pdgfra mutation (88 available)
Plekha1Gt(ROSA)82Sor mutation (1 available); any Plekha1 mutation (54 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• ovaries of females older than 8 weeks exhibit a hyperplastic stroma, containing multiple atretic follicles
• reduction in numbers of vascular smooth muscle cells in the ovaries
• decrease in numbers of later stage antral follicles
• reduction in theca cells
• uterus is hypoplastic, with major uterine layers present but underdeveloped
• little or no ovulation
• 71% of females are sterile

homeostasis/metabolism

endocrine/exocrine glands
• ovaries of females older than 8 weeks exhibit a hyperplastic stroma, containing multiple atretic follicles
• reduction in numbers of vascular smooth muscle cells in the ovaries
• decrease in numbers of later stage antral follicles
• reduction in theca cells

cardiovascular system
• reduction in numbers of vascular smooth muscle cells in the ovaries

muscle
• reduction in numbers of vascular smooth muscle cells in the ovaries




Genotype
MGI:3823001
cx6
Allelic
Composition
Pdgfratm1Sor/Pdgfra+
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor
Genetic
Background
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfratm1Sor mutation (0 available); any Pdgfra mutation (88 available)
TiparpGt(ROSA)79Sor mutation (1 available); any Tiparp mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system




Genotype
MGI:3823017
cx7
Allelic
Composition
Pdgfratm1Sor/Pdgfra+
Sgpl1Gt(ROSA)78Sor/Sgpl1Gt(ROSA)78Sor
Genetic
Background
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfratm1Sor mutation (0 available); any Pdgfra mutation (88 available)
Sgpl1Gt(ROSA)78Sor mutation (1 available); any Sgpl1 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system




Genotype
MGI:3823020
cx8
Allelic
Composition
Pdgfratm1Sor/Pdgfra+
Schip1Gt(ROSA)77Sor/Schip1Gt(ROSA)77Sor
Genetic
Background
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfratm1Sor mutation (0 available); any Pdgfra mutation (88 available)
Schip1Gt(ROSA)77Sor mutation (1 available); any Schip1 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• ovaries of females older than 8 weeks exhibit a hyperplastic stroma, containing multiple atretic follicles
• reduction in numbers of vascular smooth muscle cells in the ovaries
• number and incidence of corpora lutea are reduced
• decrease in numbers of later stage antral follicles
• reduction in theca cells
• uterus is hypoplastic, with major uterine layers present but underdeveloped
• little or no ovulation
• 45% of females are sterile

homeostasis/metabolism

endocrine/exocrine glands
• ovaries of females older than 8 weeks exhibit a hyperplastic stroma, containing multiple atretic follicles
• reduction in numbers of vascular smooth muscle cells in the ovaries
• number and incidence of corpora lutea are reduced
• decrease in numbers of later stage antral follicles
• reduction in theca cells

cardiovascular system
• reduction in numbers of vascular smooth muscle cells in the ovaries

muscle
• reduction in numbers of vascular smooth muscle cells in the ovaries




Genotype
MGI:3823024
cx9
Allelic
Composition
2610005L07RikGt(ROSA)73Sor/2610005L07RikGt(ROSA)73Sor
Pdgfratm1Sor/Pdgfra+
Genetic
Background
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
2610005L07RikGt(ROSA)73Sor mutation (1 available); any 2610005L07Rik mutation (13 available)
Pdgfratm1Sor mutation (0 available); any Pdgfra mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• ovaries of females older than 8 weeks exhibit a hyperplastic stroma, containing multiple atretic follicles
• reduction in numbers of vascular smooth muscle cells in the ovaries
• number and incidence of corpora lutea are reduced
• decrease in numbers of later stage antral follicles
• reduction in theca cells
• uterus is hypoplastic, with major uterine layers present but underdeveloped
• little or no ovulation
• 35% of females are sterile

homeostasis/metabolism

endocrine/exocrine glands
• ovaries of females older than 8 weeks exhibit a hyperplastic stroma, containing multiple atretic follicles
• reduction in numbers of vascular smooth muscle cells in the ovaries
• number and incidence of corpora lutea are reduced
• decrease in numbers of later stage antral follicles
• reduction in theca cells

cardiovascular system
• reduction in numbers of vascular smooth muscle cells in the ovaries

muscle
• reduction in numbers of vascular smooth muscle cells in the ovaries





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory