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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Elof1tm1.1(KOMP)Vlcg
targeted mutation 1.1, Velocigene
MGI:5569949
Summary 3 genotypes


Genotype
MGI:6358104
hm1
Allelic
Composition
Elof1tm1.1(KOMP)Vlcg/Elof1tm1.1(KOMP)Vlcg
Genetic
Background
B6N(Cg)-Elof1tm1.1(KOMP)Vlcg/J
Cell Lines 13491A-G1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Elof1tm1.1(KOMP)Vlcg mutation (1 available); any Elof1 mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Elof1tm1.1(KOMP)Vlcg/Elof1tm1.1(KOMP)Vlcg mice exhibit embryonic lethality, with the expected number of embryos at E7.5 that arrest prior to gastrulation, but no embryos at E9.5. Embryos are smaller at E7.5 with no primitive streak or node.

mortality/aging
• homozygous embryos are recovered in expected Mendelian ratios at E7.5 and E8.5; however, no embryos are obtained at E9.5, E12.5 or E18.5
• homozygous embryos are recovered in expected ratios at E7.5 but arrest prior to gastrulation; no homozygous embryos are recovered at E9.5

embryo
• by E8.5, all structures typical of wild-type embryos, including headfolds, heart, somites and allantois, are missing
• however, most embryos display a clear extra-embryonic/embryonic boundary indicating that pre-gastrulation events leading to egg cylinder formation are normal
• embryos fail to initiate gastrulation; even at E8.5, features typical of gastrulating embryos (primitive streak, node, and early headfolds) are not observed
• all embryos show morphological defects resulting in developmental failure (J:277394)
• embryos arrest prior to gastrulation (J:279207)
• at E7.5, embryos resemble E6.5 wild-type controls in overall size and shape
• by E8.5, embryos have increased in size (relative to E7.5) but remain smaller than wild-type controls
• at E7.5, embryos are smaller than wild-type controls
• at E7.5, many embryos show an abnormal buildup of cells in the embryonic portion of the embryo, while others show a severe reduction of the proximal-distal length of the embryo proper
• the embryonic compartments are filled with small and abnormally rounded cells
• epiblast cells appear to adopt a uniform atypical shape
• at E7.5, no obvious Oct4+ cells are observed in the epiblast except for a subset of distally located rounded cells
• at E7.5, significantly fewer proliferation marker phospho-histoneH3-positive (PH3+) cells are observed; only mutant cells that are PH3+ are those that are also Oct4+
• no head folds are observed even at E8.5 (J:277394)
• no head folds are present at E7.5 (J:279207)
• no embryonic node is observed at E8.5 (J:277394)
• no embryonic node is present at E7.5 (J:279207)
• at E7.5, Brachyury (T) expression is absent indicating failure of primitive streak initiation (J:277394)
• at E7.5, no molecular or morphological evidence of primitive streak formation is observed (J:279207)
• at E8.5
• the extra-embryonic compartments are filled with small and abnormally rounded cells
• at E8.5

growth/size/body
• at E7.5, embryos resemble E6.5 wild-type controls in overall size and shape
• by E8.5, embryos have increased in size (relative to E7.5) but remain smaller than wild-type controls
• at E7.5, embryos are smaller than wild-type controls

cellular
• at E7.5, significantly fewer proliferation marker phospho-histoneH3-positive (PH3+) cells are observed; only mutant cells that are PH3+ are those that are also Oct4+

cardiovascular system
• at E8.5




Genotype
MGI:7738859
hm2
Allelic
Composition
Elof1tm1.1(KOMP)Vlcg/Elof1tm1.1(KOMP)Vlcg
Genetic
Background
B6N(Cg)-Elof1tm1.1(KOMP)Vlcg/J
Cell Lines 13491A-G1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Elof1tm1.1(KOMP)Vlcg mutation (1 available); any Elof1 mutation (5 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:5757041
ht3
Allelic
Composition
Elof1tm1.1(KOMP)Vlcg/Elof1+
Genetic
Background
B6N(Cg)-Elof1tm1.1(KOMP)Vlcg/J
Cell Lines 13491A-G1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Elof1tm1.1(KOMP)Vlcg mutation (1 available); any Elof1 mutation (5 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological

cardiovascular system

growth/size/body

homeostasis/metabolism





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