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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Erbb3tm1Gne
targeted mutation 1, Genentech
MGI:1928828
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Erbb3tm1Gne/Erbb3tm1Gne involves: 129S2/SvPas * C57BL/6 MGI:2171460
ht2
Erbb3m3329Ddg/Erbb3tm1Gne involves: 129S2/SvPas * C57BL/6 MGI:4455313


Genotype
MGI:2171460
hm1
Allelic
Composition
Erbb3tm1Gne/Erbb3tm1Gne
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Erbb3tm1Gne mutation (0 available); any Erbb3 mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

endocrine/exocrine glands
• no chromaffin cells were detected
• at E13.5, the pancreas was not as developed as controls
• thinned mesenchyme at variable penetrance

cardiovascular system
• differentiation and thinckening of the myocardium at E13.5 was reduced compared to controls
• trabeculation is mildly affected
• hypoplastic valves with little additional development after E13.5
• valves appear incapable of supporting cardiac function
• blood reflux through the valves is apparent at E13.5

nervous system
• ectopic dopaminergic neurons are present in the mesencephalic tegmental neuroepithelium due to failure to migrate
• no chromaffin cells were detected
• enteric ganglia in the forming gut are greatly reduced
• absence of differentiated mesenchyme dorsal to the cerebellum
• the neuroepithelial layer surrounding the fourth ventricle remained rudimentary
• the tectal neuroepithelium failed to differentiate and stratify
• isthmus neuroepithelium was pyknotic
• sometimes, the tectal neuroepthelium was infolded near the cerebellum
• the tegmental neuroepithelium was developmentally delayed
• the midbrain flexure developed abnormally
• the entire brain ventricular system failed to enlarge, probably due to reduced or absent cerebrospinal fluid production
• the lateral and the fourth ventricles exhibit an absence of fingerlike projections and a long base projection compared to controls
• the mesenchyme separating the hypothalamus and ventral tegmentum and pons was thickened and abnormally oriented
• thinned neocortex
• very little differentiation and the entire plate was misshapen
• observed at E13.5
• Schwann cells are present in reduced numbers on the trigeminal ganglion and dorsal root ganglia
• few cells are present along the surface of axon projections from the dorsal root ganglia or cranial nerves
• mispositioned ventrally and with abnormal nerve projections
• absence of mandibular portion of the ganglion
• abnormal and disorganized nerve projections
• normal geniculate ganglion
• normal vestibulocochlear ganglion
• the ventral root constriction was absent

digestive/alimentary system
• normal organization of stomach layers
• the mesenchyme and the epithelial lining appear thinned

muscle
• differentiation and thinckening of the myocardium at E13.5 was reduced compared to controls
• trabeculation is mildly affected

embryo
• the neuroepithelial layer surrounding the fourth ventricle remained rudimentary
• the tectal neuroepithelium failed to differentiate and stratify
• isthmus neuroepithelium was pyknotic
• sometimes, the tectal neuroepthelium was infolded near the cerebellum
• the tegmental neuroepithelium was developmentally delayed

cellular
• ectopic dopaminergic neurons are present in the mesencephalic tegmental neuroepithelium due to failure to migrate




Genotype
MGI:4455313
ht2
Allelic
Composition
Erbb3m3329Ddg/Erbb3tm1Gne
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Erbb3m3329Ddg mutation (1 available); any Erbb3 mutation (47 available)
Erbb3tm1Gne mutation (0 available); any Erbb3 mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mice exhibit the same defasciculation in trigeminal and spinal nerves observed in either single homozygote
• mice exhibit the same defasciculation in the trigeminal nerve observed in either single homozygote
• mice exhibit the same defasciculation in spinal nerves observed in either single homozygote

cellular
• mice exhibit the same defasciculation in trigeminal and spinal nerves observed in either single homozygote





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory