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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
TiparpGt(ROSA)79Sor
gene trapped 79, Philippe Soriano
MGI:3526866
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6) MGI:3822998
hm2
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor involves: 129S4/SvJaeSor MGI:3717120
hm3
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6J MGI:6449734
cx4
Pdgfrbtm1Sor/Pdgfrb+
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor
either: (involves: 129S4/SvJaeSor * 129S7/SvEvBrd) or (involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6) MGI:3823002
cx5
Pdgfratm1Sor/Pdgfra+
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6) MGI:3823001
cx6
Plekha1Gt(ROSA)82Sor/Plekha1Gt(ROSA)82Sor
TiparpGt(ROSA)79Sor/Tiparp+
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6) MGI:3823034
cx7
Pdgfratm2Sor/Pdgfra+
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor
involves: 129S4/SvJaeSor MGI:3717135


Genotype
MGI:3822998
hm1
Allelic
Composition
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:
TiparpGt(ROSA)79Sor mutation (1 available); any Tiparp mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• females exhibit an abnormally large number of corpora lutea
• females exhibit an abnormally large number of late stage antral follicles
• occasionally develop hemorrhagic cysts
• the few observed pregnancies last longer, between 21 and 23 days instead of 19 days, however pups are either born dead or mothers show declining health and were sacrificed
• length of estrus cycle is protracted, lasting up to 4 days instead of the normal 13 hours
• smaller litter size (2.8 vs 9.3 in wild type)

homeostasis/metabolism

endocrine/exocrine glands
• females exhibit an abnormally large number of corpora lutea
• females exhibit an abnormally large number of late stage antral follicles
• occasionally develop hemorrhagic cysts

growth/size/body
• occasionally develop hemorrhagic cysts




Genotype
MGI:3717120
hm2
Allelic
Composition
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor
Genetic
Background
involves: 129S4/SvJaeSor
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
TiparpGt(ROSA)79Sor mutation (1 available); any Tiparp mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 32% of mice die by week 2

skeleton
• abnormal neural crest derived and thoracic skeleton
• 55% of mice have reduced calvarial bones at the midline with increases in the gaps between frontal bones
• increases in the gaps between frontal bones
• 78% of homozygous mice have smaller presphenoid bone processes that are less extended towards the midline
• 78% of homozygous mice have smaller palatine bone processes that are less extended towards the midline
• 44% of mice have sternum defects including asymmetric or additional fusion of ribs and gaps in the sternum

renal/urinary system
• kidney is swollen in sections and blood filled
• glomeruli are often degraded
• excess smooth muscle cells are found in the glomeruli

hematopoietic system
• by week 6
• by week 6
• an increase in immature red blood cells is observed compared to wild-type mice

homeostasis/metabolism

cardiovascular system
• at E11.5-E18.5

muscle
• excess smooth muscle cells are found in the glomeruli

immune system
• kidney is swollen in sections and blood filled

craniofacial
• 55% of mice have reduced calvarial bones at the midline with increases in the gaps between frontal bones
• increases in the gaps between frontal bones
• 78% of homozygous mice have smaller presphenoid bone processes that are less extended towards the midline
• irregularities in fusion persist into adulthood
• 78% of homozygous mice have smaller palatine bone processes that are less extended towards the midline
• snout is shorter and wider than in wild-type mice
• snout is shorter and wider than in wild-type mice

digestive/alimentary system
• irregularities in fusion persist into adulthood
• 78% of homozygous mice have smaller palatine bone processes that are less extended towards the midline

growth/size/body
• irregularities in fusion persist into adulthood
• 78% of homozygous mice have smaller palatine bone processes that are less extended towards the midline
• snout is shorter and wider than in wild-type mice
• snout is shorter and wider than in wild-type mice

respiratory system




Genotype
MGI:6449734
hm3
Allelic
Composition
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
TiparpGt(ROSA)79Sor mutation (1 available); any Tiparp mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• dioxin-treated mice show reduced fasting serum glucose levels from day 1 to 3
• dioxin-treated mice show increased serum alanine aminotransferase activity
• mice exhibit increased sensitivity to dioxin-induced lethality, with mice becoming moribund between 3 and 5 days
• mice exhibit increased sensitivity to dioxin-induced toxicity, showing decreased body weight, reduced fasting serum glucose levels, induction of thymic involution, hepatomegaly, liver degeneration, and increased hepatosteatosis

mortality/aging
• mice exhibit increased sensitivity to dioxin-induced lethality, with mice becoming moribund between 3 and 5 days

endocrine/exocrine glands
• dioxin-treatment induces thymic involution

growth/size/body
• dioxin-treated mice show reduced body weight on day 3 due to decreased food intake on days 1 and 2
• dioxin-treated mice show hepatomegaly

hematopoietic system
• dioxin-treatment induces thymic involution

immune system
• dioxin-treatment induces thymic involution

liver/biliary system
• dioxin-treated mice show hepatomegaly
• mice exhibit increased dioxin-induced hepatosteatosis, showing increases in intrahepatic triglycerides, cholesterol and free fatty acids levels
• expression analysis suggest that increased sensitivity to dioxin-induced hepatosteatosis is due to increased uptake of circulating lipids rather than increased hepatic lipogenesis
• dioxin-treated mice show increased degenerative changes in the liver, including focal inflammatory infiltration and increased cytoplasmic clearing of periportal hepatocytes on day 1 and microvesicular steatosis with regions of focal vacuolation on day 3
• dioxin-treated mice exhibit increased hepatic expression of Il1-beta and Cxcl2




Genotype
MGI:3823002
cx4
Allelic
Composition
Pdgfrbtm1Sor/Pdgfrb+
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor
Genetic
Background
either: (involves: 129S4/SvJaeSor * 129S7/SvEvBrd) or (involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfrbtm1Sor mutation (1 available); any Pdgfrb mutation (87 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:3823001
cx5
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:3823034
cx6
Allelic
Composition
Plekha1Gt(ROSA)82Sor/Plekha1Gt(ROSA)82Sor
TiparpGt(ROSA)79Sor/Tiparp+
Genetic
Background
either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plekha1Gt(ROSA)82Sor mutation (1 available); any Plekha1 mutation (54 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
N
• double mutants are fertile unlike single homozygous Plekha1 mutant mice




Genotype
MGI:3717135
cx7
Allelic
Composition
Pdgfratm2Sor/Pdgfra+
TiparpGt(ROSA)79Sor/TiparpGt(ROSA)79Sor
Genetic
Background
involves: 129S4/SvJaeSor
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pdgfratm2Sor 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
craniofacial
• distance between the frontal bones is increased compared with TiparpGt(ROSA)79Sor homozygotes and often accompanied by outgrowth of the interfrontal bone
• shorter and wider than in TiparpGt(ROSA)79Sor homozygotes
• shorter and wider than in TiparpGt(ROSA)79Sor homozygotes

skeleton
• skeletal defects are more severe than in TiparpGt(ROSA)79Sor homozygotes
• distance between the frontal bones is increased compared with TiparpGt(ROSA)79Sor homozygotes and often accompanied by outgrowth of the interfrontal bone

growth/size/body
• shorter and wider than in TiparpGt(ROSA)79Sor homozygotes
• shorter and wider than in TiparpGt(ROSA)79Sor homozygotes

respiratory system





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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory