About   Help   FAQ
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 (48 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 (48 available)
Erbb3tm1Gne mutation (0 available); any Erbb3 mutation (48 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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/19/2024
MGI 6.24
The Jackson Laboratory