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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mib1tm1Kong
targeted mutation 1, Young-Yun Kong
MGI:3603514
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mib1tm1Kong/Mib1tm1Kong either: B6.129P2-Mib1tm1Kong or (involves: 129P2/OlaHsd * FVB/N) MGI:3603810
hm2
Mib1tm1Kong/Mib1tm1Kong involves: 129P2/OlaHsd MGI:3804833
hm3
Mib1tm1Kong/Mib1tm1Kong involves: 129P2/OlaHsd * C57BL/6 MGI:3804813
cx4
Mib1tm1Kong/Mib1+
Mib2tm1Kong/Mib2tm1Kong
involves: 129P2/OlaHsd * C57BL/6 MGI:3804811
cx5
Mib1tm1Kong/Mib1tm1Kong
Mib2tm1Kong/Mib2tm1Kong
involves: 129P2/OlaHsd * C57BL/6 MGI:3804812
cx6
Mib1tm1Kong/Mib1tm1Kong
Mib2tm1Kong/Mib2+
involves: 129P2/OlaHsd * C57BL/6 MGI:3804814


Genotype
MGI:3603810
hm1
Allelic
Composition
Mib1tm1Kong/Mib1tm1Kong
Genetic
Background
either: B6.129P2-Mib1tm1Kong or (involves: 129P2/OlaHsd * FVB/N)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mib1tm1Kong mutation (0 available); any Mib1 mutation (55 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only dead or resorbed homozygous embryos are found at E11.5 - E12.5

embryo
• the second branchial arches are absent
• at E9.5 embryos are posteriorly truncated
• at E9.5 homozygous embryos are severely growth retarded
• loss of mesenchyme cells is seen in transverse sections at E9.5
• the notochord is fused to the neural tube
• seen at E9.5
• the notochord is fused to the neural tube
• at E8.5 expression data indicate that somatic polarity and oscillation are absent, with markers for the posterior half of each somite absent
• somitogenesis is irregular with some somites fused
• the yolk sac appears blistered
• the initial vascular plexus forms but the reorganization into a network of large vessels does not occur

cardiovascular system
• intersomitic vessels are absent or when present (in the anterior part of the embryo) show an irregular ladder shape
• the dorsal aorta is smaller, lacks expression of ephrin B2, and shows markedly reduced recruitment of smooth muscle cells
• the dorsal aorta and vessels in the yolk sac have decreased expression of arterial-specific markers
• the dorsal aorta and vessels in the yolk sac have decreased expression of arterial-specific markers
• vessels in the head are thin, truncated, and do not form a finely branched network
• heart looping does not occur
• at E9.5 the heart appears small and thin in transverse sections
• the pericardial sac is balloon-like
• at E9.5 embryos lack circulation

nervous system
• at E9.0 - 9.5 most of the cells in the brain are positive for markers of early neurons and almost no cells are proliferating and at E9.5 - 9.75 the neurosphere forming cells are absent and many apoptotic cells are seen in the brai
• the notochord is fused to the neural tube
• seen at E9.5

craniofacial
• the second branchial arches are absent

growth/size/body
• at E9.5 homozygous embryos are severely growth retarded

cellular
• vessels in the head are thin, truncated, and do not form a finely branched network
• at E9.0 - 9.5 most of the cells in the brain are positive for markers of early neurons and almost no cells are proliferating and at E9.5 - 9.75 the neurosphere forming cells are absent and many apoptotic cells are seen in the brai




Genotype
MGI:3804833
hm2
Allelic
Composition
Mib1tm1Kong/Mib1tm1Kong
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mib1tm1Kong mutation (0 available); any Mib1 mutation (55 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• cultures of para-aortic splanchnopleura fail to form colonies unlike wild-type cultures
• however, hematopoiesis in the yolk sac and generation of hemogenic cells are normal and culturing of para-aortic splanchnopleura on Dll1-expressing OP-9 cells restores colony forming cells

cardiovascular system
• mice exhibit a fused and disorganized aorta




Genotype
MGI:3804813
hm3
Allelic
Composition
Mib1tm1Kong/Mib1tm1Kong
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mib1tm1Kong mutation (0 available); any Mib1 mutation (55 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:3804811
cx4
Allelic
Composition
Mib1tm1Kong/Mib1+
Mib2tm1Kong/Mib2tm1Kong
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mib1tm1Kong mutation (0 available); any Mib1 mutation (55 available)
Mib2tm1Kong mutation (0 available); any Mib2 mutation (61 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice exhibit no abnormal phenotype




Genotype
MGI:3804812
cx5
Allelic
Composition
Mib1tm1Kong/Mib1tm1Kong
Mib2tm1Kong/Mib2tm1Kong
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mib1tm1Kong mutation (0 available); any Mib1 mutation (55 available)
Mib2tm1Kong mutation (0 available); any Mib2 mutation (61 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:3804814
cx6
Allelic
Composition
Mib1tm1Kong/Mib1tm1Kong
Mib2tm1Kong/Mib2+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mib1tm1Kong mutation (0 available); any Mib1 mutation (55 available)
Mib2tm1Kong mutation (0 available); any Mib2 mutation (61 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory