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Phenotypes Associated with This Genotype
Genotype
MGI:3717269
Allelic
Composition
Ptentm1Mak/Pten+
Genetic
Background
B6.129P2-Ptentm1Mak
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptentm1Mak mutation (1 available); any Pten mutation (86 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Embryonic defects in Ptentm1Mak/Pten+

mortality/aging

growth/size/body
• the majority of embryos are smaller but have normal body symmetry and development of most organ systems

embryo
• majority of embryos remain unturned
• the majority of embryos are smaller but have normal body symmetry and development of most organ systems
• severely affected (about 5%) embryos have little or no development of the major organ systems, including the heart and brachial arches
• severely affected (about 5%) embryos have asymmetrical head folds
• neural tube is open along the entire length of the embryo
• neural tube is kinked along the entire length of the embyo
• the remaining 20% of moribound embryos display other placental abnormalities including disorganization of the spongiotrophoblast layer and limited invasion of the trophoblast layer by the chorion
• the allantois fails to fuse to the chorion at E9 in 80% of dying embryos

nervous system
• neural tube is open along the entire length of the embryo
• neural tube is kinked along the entire length of the embyo

neoplasm

endocrine/exocrine glands

reproductive system


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
01/06/2026
MGI 6.24
The Jackson Laboratory