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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Aggf1Gt(PT036)Byg
gene trap PT036, BayGenomics
MGI:4122569
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Aggf1Gt(PT036)Byg/Aggf1Gt(PT036)Byg involves: 129P2/OlaHsd * C57BL/6 MGI:5882325
ht2
Aggf1Gt(PT036)Byg/Aggf1+ involves: 129P2/OlaHsd * C57BL/6 MGI:5882324


Genotype
MGI:5882325
hm1
Allelic
Composition
Aggf1Gt(PT036)Byg/Aggf1Gt(PT036)Byg
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aggf1Gt(PT036)Byg mutation (0 available); any Aggf1 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos die before E8.5




Genotype
MGI:5882324
ht2
Allelic
Composition
Aggf1Gt(PT036)Byg/Aggf1+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aggf1Gt(PT036)Byg mutation (0 available); any Aggf1 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice older than 40 weeks of age show a slightly increased rate of sudden death events
• 1/3 of embryos die before birth; 56.1% survive to birth and develop to adulthood

embryo
• yolk sacks have fewer vessels and much less vascular branching

cardiovascular system
• well-developed vasculature, particularly in the brain area, is not seen at E10.5 as in wild-type embryos
• less vessel density in lungs of 40 week or older mice compared to wild-type mice
• fewer vessels are seen in embryos
• 43.9% of embryos show an abnormal vascular phenotype
• however, hearts appear normal at E14.5 and 8 weeks of age in surviving mice
• implanted melanoma cells that develop into tumors show decreased vascular density compared to controls
• yolk sacks have fewer vessels and much less vascular branching
• about 35% of adult mice display hemorrhages in the brain, spleen, and lungs
• lungs of 40 week or older mice show leakage of blood cells
• some embryos exhibit severe hemorrhages, especially in the cranial region
• microvascular endothelial cells (MECs) show decreased capability to form capillary tubes
• wound-healing scratch assays show that migration of MECs is decreased
• reduced capillary tube formation by MECs is rescued by overexpression of constitutively active AKT or treatment with recombinant AGGF1
• vascular permeability of 50-60 week old mice is 2-fold greater than in wild-type mice

behavior/neurological
• mice older than 40 weeks of age show signs of fatigue

cellular
• wound-healing scratch assays show that migration of MECs is decreased

neoplasm
• implanted melanoma cells that develop into tumors show decreased vascular density compared to controls
• tumor growth of both B16F10 and B16F0 melanoma cells is inhibited compared to growth in wild-type mice

nervous system
• well-developed vasculature, particularly in the brain area, is not seen at E10.5 as in wild-type embryos
• some embryos exhibit severe hemorrhages, especially in the cranial region

respiratory system
• less vessel density in lungs of 40 week or older mice compared to wild-type mice
• lungs of 40 week or older mice show leakage of blood cells
• wound-healing scratch assays show that migration of MECs is decreased





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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
11/12/2024
MGI 6.24
The Jackson Laboratory