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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Scfd1em1(IMPC)Tcp
endonuclease-mediated mutation 1, The Centre for Phenogenomics
MGI:6383384
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Scfd1em1(IMPC)Tcp/Scfd1em1(IMPC)Tcp C57BL/6N-Scfd1em1(IMPC)Tcp/Cmmr MGI:6493078
ht2
Scfd1em1(IMPC)Tcp/Scfd1+ C57BL/6N-Scfd1em1(IMPC)Tcp/Cmmr MGI:6696888


Genotype
MGI:6493078
hm1
Allelic
Composition
Scfd1em1(IMPC)Tcp/Scfd1em1(IMPC)Tcp
Genetic
Background
C57BL/6N-Scfd1em1(IMPC)Tcp/Cmmr
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scfd1em1(IMPC)Tcp mutation (2 available); any Scfd1 mutation (34 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype

Scfd1em1(IMPC)Tcp/Scfd1em1(IMPC)Tcp mice exhibit embryonic lethality, with embryos recovered at E3.5 as blastocysts but not at E7.5. In vitro, some blastocysts fail to hatch from the zona pellucida and do not form outgrowths while others do hatch but form outgrowths with no inner cell mass and dispersed trophectoderm.

embryo
• in vitro outgrowth assays show that some blastocysts fail to hatch from the zona pellucida after 3 days in culture
• in vitro, some blastocysts do hatch from the zona but form outgrowths with no apparent inner cell mass (ICM) after 3 days in culture
• in vitro, blastocysts that do hatch form outgrowths with no apparent ICM and dispersed trophectoderm (TE) after 3 days in culture

mortality/aging
• although blastocyst-like embryos are present in expected Mendelian ratios at E3.5, no homozygous embryos are recovered at E7.5
• however, excess resorption sites suggest that embryos elicit a decidual response in vivo

reproductive system
• in vitro, some blastocysts fail to hatch and do not form outgrowths after 3 days in culture




Genotype
MGI:6696888
ht2
Allelic
Composition
Scfd1em1(IMPC)Tcp/Scfd1+
Genetic
Background
C57BL/6N-Scfd1em1(IMPC)Tcp/Cmmr
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scfd1em1(IMPC)Tcp mutation (2 available); any Scfd1 mutation (34 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system

integument





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory