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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Robo2
roundabout guidance receptor 2
MGI:1890110
27 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Pcdhgtm2Xzw/Pcdhgtm2Xzw
Robo2tm1Rilm/Robo2tm1Rilm
involves: 129S7/SvEvBrd * C57BL/6 * CD-1
abnormal gait J:221288
abnormal Purkinje cell dendrite morphology J:221288
normal behavior/neurological phenotype J:221288
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Mrt/Robo2tm1Mrt
involves: 129P2/OlaHsd
abnormal axon guidance J:119469
abnormal diaphragm morphology J:193400
abnormal dorsal aorta morphology J:193400
abnormal foregut morphology J:193400
abnormal olfactory tract morphology J:119469
abnormal spinal cord ventral commissure morphology J:194150
abnormal stomach position or orientation J:193400
absent gastric milk in neonates J:193400
cyanosis J:193400
decreased cell migration J:193400
esophagus hypoplasia J:193400
neonatal lethality, complete penetrance J:193400
respiratory failure J:193400
short trachea J:193400
small esophagus J:193400
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Mrt/Robo2tm1Mrt
involves: 129P2/OlaHsd * C57BL/6 * CD-1
abnormal anterior commissure morphology J:120131
abnormal axon guidance J:120131
abnormal dorsal telencephalic commissure morphology J:120131
abnormal innervation J:120131
decreased corpus callosum size J:120131
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Rilm/Robo2tm1Rilm
Shhtm1(EGFP/cre)Cjt/Shh+
involves: 129
no abnormal phenotype detected J:193400
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Rilm/Robo2tm1Rilm
Tbx4tm1(cre)Tmj/Tbx4+
involves: 129
no abnormal phenotype detected J:193400
Robo1tm1Matl/Robo1tm1Matl
Robo2tm1Rilm/Robo2tm1Rilm
Twist2tm1(cre)Dor/Twist2+
involves: 129 * 129X1/SvJ
abnormal foregut morphology J:193400
diaphragmatic hernia J:193400
neonatal lethality J:193400
respiratory failure J:193400
small esophagus J:193400
Robo2tm1Mrt/Robo2tm1Mrt
Robo3tm1Matl/Robo3tm1Matl
involves: 129/Sv * CD-1
abnormal axon guidance J:89438
Robo2tm1Rilm/Robo2tm1Rilm
Or5d18tm1.1Jfcl/?
Omptm1(cre)Jae/Omp+
involves: 129 * 129S1/Sv
abnormal olfactory bulb morphology J:173325
Robo2tm1Rilm/Robo2tm1Rilm
Or8a1btm4Mom/?
Omptm1(cre)Jae/Omp+
involves: 129 * 129P2/OlaHsd * 129S1/Sv
abnormal olfactory bulb morphology J:173325
Robo2tm1Rilm/Robo2tm1Rilm
Or51b4tm1.1Jfcl/?
Omptm1(cre)Jae/Omp+
involves: 129 * 129S1/Sv
normal nervous system phenotype J:173325

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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
04/16/2024
MGI 6.23
The Jackson Laboratory