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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Stt3bem1(IMPC)J
endonuclease-mediated mutation 1, Jackson
MGI:6188000
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Stt3bem1(IMPC)J/Stt3bem1(IMPC)J C57BL/6NJ-Stt3bem1(IMPC)J/Mmjax MGI:6493134
ht2
Stt3bem1(IMPC)J/Stt3b+ C57BL/6NJ-Stt3bem1(IMPC)J/Mmjax MGI:6493133


Genotype
MGI:6493134
hm1
Allelic
Composition
Stt3bem1(IMPC)J/Stt3bem1(IMPC)J
Genetic
Background
C57BL/6NJ-Stt3bem1(IMPC)J/Mmjax
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Stt3bem1(IMPC)J mutation (2 available); any Stt3b mutation (39 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype

Stt3bem1(IMPC)J/Stt3bem1(IMPC)J (-/-) embryos at E9.5 are often small and occasionally show cardiac or pericardial edema. E10.5 mutants are developmentally delayed, show abnormal heart and yolk sac morphology, and abnormal heart shape and branchial arches.

cardiovascular system
• by E10.5, all homozygous embryos show abnormal heart morphology, including cardiac and/or pericardial edema
• at E9.5, homozygous embryos occasionally exhibit pericardial edema but most remain otherwise normal
• by E10.5, all homozygous embryos display cardiac and/or pericardial edema

craniofacial
• by E10.5, all homozygous embryos show abnormal branchial arches
• by E10.5, all homozygous embryos show abnormal head shape

embryo
• by E10.5, all homozygous embryos show abnormal branchial arches
IMPC - JAX (J:211773)
MGI
• by E10.5, many homozygous embryos are developmentally delayed relative to control littermates (J:374598)
• however, homozygous embryos are normal at E8.5; by E9.5, germ layer patterning is normal, and almost all homozygous embryos have completed turning (J:374598)
• at E9.5, homozygous embryos are often small but still within the expected range
• at E9.5 and E10.5, placentas exhibit multiple labyrinth zone defects
• at E9.5, the Tfeb+ labyrinth trophoblast layer is of normal thickness, but Tfeb signal intensity appears elevated, suggesting an increased density of Tfeb+ cells
• by E10.5, the Tfeb+ labyrinth trophoblast layer is slightly reduced in thickness, but signal intensity remains elevated
• by E10.5, all homozygous embryos show abnormal yolk sac morphology
• Gcm1+ chorioallantoic branching is reduced at E9.5 and severely impaired by E10.5

growth/size/body
• by E10.5, all homozygous embryos show abnormal head shape
IMPC - JAX (J:211773)
MGI
• by E10.5, many homozygous embryos are developmentally delayed relative to control littermates (J:374598)
• however, homozygous embryos are normal at E8.5; by E9.5, germ layer patterning is normal, and almost all homozygous embryos have completed turning (J:374598)
• at E9.5, homozygous embryos are often small but still within the expected range

homeostasis/metabolism
• at E9.5, homozygous embryos occasionally exhibit pericardial edema but most remain otherwise normal
• by E10.5, all homozygous embryos display cardiac and/or pericardial edema
• at E9.5, homozygous embryos occasionally exhibit cardiac edema but most remain otherwise normal
• by E10.5, all homozygous embryos display cardiac and/or pericardial edema

mortality/aging
• homozygous embryos are present in Mendelian ratios at E8.5-E10.5; all homozygous embryos recovered at E11.5 are dying/undergoing resorption




Genotype
MGI:6493133
ht2
Allelic
Composition
Stt3bem1(IMPC)J/Stt3b+
Genetic
Background
C57BL/6NJ-Stt3bem1(IMPC)J/Mmjax
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Stt3bem1(IMPC)J mutation (2 available); any Stt3b mutation (39 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological

hematopoietic system

homeostasis/metabolism





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last database update
01/06/2026
MGI 6.24
The Jackson Laboratory