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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Aiptm1Bra
targeted mutation 1, Christopher A Bradfield
MGI:3819941
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Aiptm1Bra/Aiptm1Bra involves: 129S4/SvJaeSor * C57BL/6 MGI:3819951
ht2
Aiptm1Bra/Aip+ Not Specified MGI:4867899


Genotype
MGI:3819951
hm1
Allelic
Composition
Aiptm1Bra/Aiptm1Bra
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aiptm1Bra mutation (0 available); any Aip mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Vessel caliber is decreased in Aiptm1Bra/Aiptm1Bra fetuses

mortality/aging
• at E15-17, the wild-type/heterozygote/homozygote frequency is 1:1.6:0.3, indicating further lethality
• at E18-19, the wild-type/heterozygote/homozygote frequency is 1:1.6:0.08, indicating lethality in late development
• first loss of embryos occurs between E10 and E14, with a wild-type/heterozygote/homozygote frequency of 1:1.5:0.4

growth/size/body
• seen in some mutants at E81.5

embryo
• a few mutants show decreased number and caliber of vessels in yolk sacs

cardiovascular system
• a few mutants show decreased number and caliber of vessels in yolk sacs
• 57% of surviving embryos between E13.5 and E14.5 exhibit a double-outlet right ventricle
• 71% penetrance of a ventricular septal defect (VSD) by E14.5; most mutants with double-outlet right ventricle exhibit the VSD
• 71% of mutants exhibit pronounced pericardial edema by E14.5
• by E14.5-15, surviving mutants show a decreased volume of blood in vessels in the head and extremities
• some mutants exhibit hemorrhaging between E14.5 and E18.5

homeostasis/metabolism
• 71% of mutants exhibit pronounced pericardial edema by E14.5

integument
• mutants are paler at E14.5-15
• some mutants exhibit petechiae along the surface of their bodies near the head and upper torso between E14.5 and E18.5




Genotype
MGI:4867899
ht2
Allelic
Composition
Aiptm1Bra/Aip+
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aiptm1Bra mutation (0 available); any Aip mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• in 56% of mice

liver/biliary system

cellular
• in 56% of mice





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)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory