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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rhot1tm1.2Jmsu
targeted mutation 1.2, Janet M Shaw
MGI:5619348
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rhot1tm1.2Jmsu/Rhot1tm1.2Jmsu involves: 129 * 129S1/Sv * C57BL/6 * SJL MGI:5619349
cn2
Mnx1tm4(cre)Tmj/Mnx1+
Rhot1tm1.1Jmsu/Rhot1tm1.2Jmsu
involves: 129 * 129S1/Sv * C57BL/6 * SJL MGI:5619357


Genotype
MGI:5619349
hm1
Allelic
Composition
Rhot1tm1.2Jmsu/Rhot1tm1.2Jmsu
Genetic
Background
involves: 129 * 129S1/Sv * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rhot1tm1.2Jmsu mutation (0 available); any Rhot1 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die shortly after birth

respiratory system
• mice exhibit unexpanded lungs upon postmortem autopsy
• however, lungs exhibit no abnormalities

nervous system
• the central neural respiratory network located in the brainstem, which includes cranial motor neurons of the nucleus ambiguous, is absent at E15.5 and E18.5
• disorganization of the neurons that innervate facial muscles
• the central neural respiratory network located in the brainstem, which includes cranial motor neurons of the nucleus ambiguous, is absent at E15.5 and E18.5
• mice exhibit fewer motor neurons in the cervical spinal cord at levels C3-C5
• phrenic nerve exhibits fewer axonal branches

cellular
• motile mitochondria in cortical axons spend less time in motion compared to wild-type mitochondria
• mitochondria in axons exhibits a 4-fold reduction in overall retrograde velocity, however, anterograde velocity is no different
• 2-fold reduction in retrograde run length in cortical neurons indicates, that retrograde axonal mitochondrial movement is affected
• mitochondrial respiration is intact and mitochondrial membrane potential is not altered
• mitochondria in MEFs is clustered around the nucleus and is absent from filopodia unlike in wild-type MEFs which show distribution throughout the cytoplasm and in filopodia

homeostasis/metabolism

cardiovascular system
N
• mice exhibit normal cardiac function before birth as indicated by normal fetal cardiac ultrasound at E18.5




Genotype
MGI:5619357
cn2
Allelic
Composition
Mnx1tm4(cre)Tmj/Mnx1+
Rhot1tm1.1Jmsu/Rhot1tm1.2Jmsu
Genetic
Background
involves: 129 * 129S1/Sv * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mnx1tm4(cre)Tmj mutation (2 available); any Mnx1 mutation (29 available)
Rhot1tm1.1Jmsu mutation (0 available); any Rhot1 mutation (44 available)
Rhot1tm1.2Jmsu mutation (0 available); any Rhot1 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice do not exhibit any obvious phenotypes





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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
11/12/2024
MGI 6.24
The Jackson Laboratory