Phenotypes Associated with This Genotype

Genotype
MGI:3806652

• Allelic Composition: Foxa2^{tm2(cre/Esr1*)Moon}/Foxa2^{tm2(cre/Esr1*)Moon}
• Genetic Background: Not Specified

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

mortality/aging

embryonic lethality, complete penetrance ( J:130990 )

• occurs to all embryos

cardiovascular system

delayed heart development ( J:130990 )

• delayed development is noted in E9.5 embryos

craniofacial

abnormal craniofacial development ( J:130990 )

• defects are noted in cranium development in E9.5 embryos