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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Robo2tm1Mrt
targeted mutation 1, Gail R Martin
MGI:3043127
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Robo2tm1Mrt/Robo2tm1Mrt involves: 129P2/OlaHsd MGI:5522717
hm2
Robo2tm1Mrt/Robo2tm1Mrt involves: 129P2/OlaHsd * 129/Sv * C57BL/6 * CD-1 MGI:3043154
hm3
Robo2tm1Mrt/Robo2tm1Mrt involves: 129P2/OlaHsd * C57BL/6 MGI:5522686
hm4
Robo2tm1Mrt/Robo2tm1Mrt Not Specified MGI:3043185
cx5
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Mrt/Robo2tm1Mrt
involves: 129P2/OlaHsd MGI:5470528
cx6
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Mrt/Robo2tm1Mrt
involves: 129P2/OlaHsd * C57BL/6 * CD-1 MGI:5522691
cx7
Robo2tm1Mrt/Robo2tm1Mrt
Robo3tm1Matl/Robo3tm1Matl
involves: 129/Sv * CD-1 MGI:3043210


Genotype
MGI:5522717
hm1
Allelic
Composition
Robo2tm1Mrt/Robo2tm1Mrt
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Robo2tm1Mrt mutation (2 available); any Robo2 mutation (101 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• thinner and spread along the ventrolateral surface of the telencephalon at E18




Genotype
MGI:3043154
hm2
Allelic
Composition
Robo2tm1Mrt/Robo2tm1Mrt
Genetic
Background
involves: 129P2/OlaHsd * 129/Sv * C57BL/6 * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Robo2tm1Mrt mutation (2 available); any Robo2 mutation (101 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• almost all homozygotes fail to survive after birth

renal/urinary system
• multiple ureters arising from a single kidney are seen with 6/14 kidneys having 3 ureters, 6/14 having 2 ureters, and 2 having only 1 ureter
• most of the ureters remain connected to the nephric duct rather than undergoing remodeling to connect to the bladder




Genotype
MGI:5522686
hm3
Allelic
Composition
Robo2tm1Mrt/Robo2tm1Mrt
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Robo2tm1Mrt mutation (2 available); any Robo2 mutation (101 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• appears to be ventrally displaced and corticofugal axons abnormally defasciculate in some mice at E18.5
• at E18.5, a few corticofugal axons are ventrally displaced reaching the ventral midline at the level of the anterior commissure and occasional bundles of cortical fibers are found in the dorsal thalamus
• at E18.5, some thalamocortical fibers fail to reach the telencephalon and instead grow toward the ventral diencephalon and invade the hypothalamu




Genotype
MGI:3043185
hm4
Allelic
Composition
Robo2tm1Mrt/Robo2tm1Mrt
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Robo2tm1Mrt mutation (2 available); any Robo2 mutation (101 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• commissural axons remain tightly apposed to the floor plate rather than moving into more dorsal longitudinal tracts
• the lateral funiculus (white matter tract) is foreshortened in homozygous mutants compared to wild-type mice as a result of abnormal commissural axon growth

cellular
• commissural axons remain tightly apposed to the floor plate rather than moving into more dorsal longitudinal tracts




Genotype
MGI:5470528
cx5
Allelic
Composition
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Mrt/Robo2tm1Mrt
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Robo1tm1Matl mutation (2 available); any Robo1 mutation (87 available)
Robo2tm1Mrt mutation (2 available); any Robo2 mutation (101 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• die within minutes of birth

homeostasis/metabolism

respiratory system
• slightly shorter
• lungs fail to inflate

nervous system
• olfactory bulb axons from E14 explants are not repelled by SLIT proteins
• highly defasciculated into small axonal bundles fanned all over the ventral side of the telencephalon, at E15.5 and E18
• a subset of axons originating from the lateral bulb are still present in the normal location
• at E11.5, commissural axons exhibit robust postcrossing trajectory defects with failure to project to the lateral portion of the funiculus and altered lateral and ventral funiculi ration compared with wild-type mice

cellular
• olfactory bulb axons from E14 explants are not repelled by SLIT proteins
• in culture, fewer E10.5 foregut cells migrate away from SLIT2 containing media

digestive/alimentary system
• mispositioning of the stomach in the thoracic instead of the abdominal cavity
• abnormal midline position detected as early as E11.5
• more prominent at E13.5 and disrupts the diaphragm
• located at the midline and protrudes through the esophageal hiatus into the thoracic cavity in neonates
• delayed separation of the foregut from the body wall
• short

muscle

behavior/neurological

cardiovascular system
• fails to fuse by E11.5




Genotype
MGI:5522691
cx6
Allelic
Composition
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Mrt/Robo2tm1Mrt
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Robo1tm1Matl mutation (2 available); any Robo1 mutation (87 available)
Robo2tm1Mrt mutation (2 available); any Robo2 mutation (101 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular

nervous system
• two large ectopic fiber bundles formed of corticocortical axons are seen on either side of the corpus callosum at E18.5
• displaced dorsally due to the presence of ectopic fiber bundles
• large bundles of ectopic fibers are seen crossing the ventral midline at the level of the anterior commissure and in the basal telencephalon at E18.5
• most corticofugal axons are diverted toward the midline
• only a few cortical axons reach the dorsal thalamus and those that do follow a more ventral trajectory
• virtually no corticospinal axons reach the diencephalon
• many thalamic axons abnormally invade the hypothalamus




Genotype
MGI:3043210
cx7
Allelic
Composition
Robo2tm1Mrt/Robo2tm1Mrt
Robo3tm1Matl/Robo3tm1Matl
Genetic
Background
involves: 129/Sv * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Robo2tm1Mrt mutation (2 available); any Robo2 mutation (101 available)
Robo3tm1Matl mutation (1 available); any Robo3 mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E11.5 embryos show no midline crossing and look identical to Robo3tm1Matl homozygous littermates

cellular
• at E11.5 embryos show no midline crossing and look identical to Robo3tm1Matl homozygous littermates





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory