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Phenotypes Associated with This Genotype
Genotype
MGI:2449029
Allelic
Composition
Dll1tm1Gos/Dll1tm1Gos
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dll1tm1Gos mutation (2 available); any Dll1 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
• tail rotation to the left in about 48% of embryos but random relative to heart looping
• severe patterning defects in paraxial mesoderm
• enlarged floor plate between E8.5 and E10.5
• some regions appear as a sheet of cells associated with the dorsal primitive gut endoderm
• reduced number of notochord cells
• rupture of surface, bulging of cells
• by late headfold stage, abnormal cell morphology disrupts symmetry
• loss of monociliated cells
• myoblasts span segment (somite) borders, indicating that borders are not maintained
• irregularly shaped segments in the trunk
• distinct dermatomes present at E10.5 but segmental arrangement of myotome and sclerotome cells is disturbed
• myoblasts sometimes span space between adjacent segments
• absence of segments in tail bud
• caudal sclerotome forms a uniform, loose, non segmental mass

nervous system
• excessive neuronal differentiation in CNS
• enlarged floor plate between E8.5 and E10.5
• hyperplastic CNS
• wide
• irregularly spaced

cardiovascular system
• heart looping to the left in about 50% of embryos
• looping is sometimes incomplete at E8.5-9.5
• severely hemorrhagic after E10

endocrine/exocrine glands
• pancreatic bud decreased in size
• composed primarily of endocrine cells

cellular
• loss of monociliated cells
• excessive neuronal differentiation in CNS


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory