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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tubb3tm1.1Ece
targeted mutation 1.1, Elizabeth C Engle
MGI:4441058
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Tubb3tm1.1Ece/Tubb3tm1.1Ece involves: 129S/SvEv * C57BL/6J MGI:4441061
ht2
Tubb3tm1.1Ece/Tubb3+ involves: 129S/SvEv * C57BL/6J MGI:4441062


Genotype
MGI:4441061
hm1
Allelic
Composition
Tubb3tm1.1Ece/Tubb3tm1.1Ece
Genetic
Background
involves: 129S/SvEv * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tubb3tm1.1Ece mutation (0 available); any Tubb3 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

nervous system
• at E11.5 to E12, guidance and branching of cranial nerves is defective compared to in wild-type mice
• mice exhibit defective guidance of commissural axons and cranial nerves compared with wild-type mice
• mice exhibit defective guidance of commissural axons and cranial nerves compared with wild-type mice
• 2 of 5 mice exhibit thin corpus callosum compared with wild-type mice
• 1 of 5 mice exhibit thick corpus callosum compared with wild-type mice
• in 2 of 5 mice
• mice exhibit a thinning and/or absent midline crossing of the anterior commissure throughout its anterior-posterior axis compared with wild-type mice
• the anterior-posterior axis appears tortuous and often has aberrant fiber projections at the midline unlike in wild-type mice
• asymmetric in some mice
• at E11.5 to E12, guidance and branching of cranial nerves is defective compared to in wild-type mice
• the oculomotor nerve fails to reach the correct muscle anlage and instead projected towards the position of the superior oblique unlike in wild-type mice
• the trigeminal nerve fails to grow and branch properly unlike in wild-type mice
• trochlear nerve growth is often stalled unlike in wild-type mice

respiratory system
• mice fail to breath normally at birth

cellular
• at E11.5 to E12, guidance and branching of cranial nerves is defective compared to in wild-type mice
• mice exhibit defective guidance of commissural axons and cranial nerves compared with wild-type mice

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
congenital fibrosis of the extraocular muscles DOID:0080143 OMIM:PS135700
J:158992




Genotype
MGI:4441062
ht2
Allelic
Composition
Tubb3tm1.1Ece/Tubb3+
Genetic
Background
involves: 129S/SvEv * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tubb3tm1.1Ece mutation (0 available); any Tubb3 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• the anterior commissure is thinner at the midline compared to in wild-type mice





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
04/23/2024
MGI 6.23
The Jackson Laboratory