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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Erbb2tm1Gne
targeted mutation 1, Genentech
MGI:1928827
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Erbb2tm1Gne/Erbb2tm1Gne either: (involves: 129S2/SvPas * BALB/c) or (involves: 129S2/SvPas * C57BL/6J) MGI:2171457


Genotype
MGI:2171457
hm1
Allelic
Composition
Erbb2tm1Gne/Erbb2tm1Gne
Genetic
Background
either: (involves: 129S2/SvPas * BALB/c) or (involves: 129S2/SvPas * C57BL/6J)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Erbb2tm1Gne mutation (0 available); any Erbb2 mutation (59 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygous embryos die around E10.5 probably from cardiovascular defects

cardiovascular system

muscle

nervous system
• the geniculate ganglion appears fused to the vestibular ganglion
• the geniculate ganglion appears fused to the vestibular ganglion
• few axons project from the geniculate toward the second branchial arch
• the petrosal ganglion appears rounded and elongated and is positioned further from the nodose ganglion than normal
• both the glossopharyngeal and superior nerve fibers emerging from the petrosal ganglion are stunted
• the posterior and mandibular portions of the trigeminal ganglion are absent and the maxillary portion is reduced in size
• scattered neurons occupy the space between the trigeminal ganglion and the geniculate ganglion
• the rootlets of the hypoglossal nerve are missing from the C1 plexus
• the vagal projections extend further ventrally than normal
• the dorsal root ganglia are unfasciculated
• ventral root projections are unfasciculated

growth/size/body





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory