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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Poglut1Gt(IST10323G11)Tigm
gene trap IST10323G11, Texas A&M Institute for Genomic Medicine
MGI:3942939
Summary 3 genotypes


Genotype
MGI:5004904
hm1
Allelic
Composition
Poglut1Gt(IST10323G11)Tigm/Poglut1Gt(IST10323G11)Tigm
Genetic
Background
involves: C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Poglut1Gt(IST10323G11)Tigm mutation (0 available); any Poglut1 mutation (61 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• at E9.5 some embryos show signs of resorption and by E10.5 all embryos are in resorption

embryo
• contain large blood sinusoids instead of the normal vascular trees
• most embryos are unturned at E9.5
• anterior ectoderm is expanded and disorganized, especially towards the midline
• the amount of mesodermal tissues seems decreased compared to wild-type controls
• posterior axis truncation at E8.0
• complete absence of the posterior parts of the embryo at E8.5
• severe growth retardation at E9.5
• fails to fold properly at E8.0 and E8.5
• unfolded at E9.5
• abnormally expanded and improperly folded neural plate at E8.0
• at E8.5 the plate fails to fold properly but continues to expand in the anterior part of the embryo
• at E8.0 and E8.5
• severe vascular remodeling defects at E8.75

cardiovascular system
• absence of intersomitic vasculature
• absence of intersomitic vasculature
• at E8.5 no vessels are detected on the dorsal side of the head
• by E9.5 disorganized vascular networks are present on the dorsal side of the head in some embryos
• absence of the dorsal aorta
• contain large blood sinusoids instead of the normal vascular trees
• at E9.5 the cardiogenic plates are unfused
• absence of heart rudiments at E8.0 and E8.5
• at E9.5 the cardiogenic plates are still unfused

nervous system
• abnormally expanded and improperly folded neural plate at E8.0
• at E8.5 the plate fails to fold properly but continues to expand in the anterior part of the embryo

growth/size/body
• severe growth retardation at E9.5




Genotype
MGI:5004906
cx2
Allelic
Composition
Jag1tm1Grid/Jag1+
Poglut1Gt(IST10323G11)Tigm/Poglut1+
Genetic
Background
B6.Cg-Jag1tm1Grid Poglut1Gt(IST10323G11)Tigm
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Jag1tm1Grid mutation (1 available); any Jag1 mutation (78 available)
Poglut1Gt(IST10323G11)Tigm mutation (0 available); any Poglut1 mutation (61 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
liver/biliary system
• severe decrease in the number of biliary cells in the periportal regions at P0
• bile duct paucity at P0

endocrine/exocrine glands
• bile duct paucity at P0




Genotype
MGI:5004912
cx3
Allelic
Composition
Notch2tm3.1Grid/Notch2+
Poglut1Gt(IST10323G11)Tigm/Poglut1+
Genetic
Background
B6.Cg-Notch2tm3.1Grid Poglut1Gt(IST10323G11)Tigm
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Notch2tm3.1Grid mutation (0 available); any Notch2 mutation (99 available)
Poglut1Gt(IST10323G11)Tigm mutation (0 available); any Poglut1 mutation (61 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
liver/biliary system
N
• do not show bile duct abnormalities





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