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Phenotypes Associated with This Genotype
Genotype
MGI:2175169
Allelic
Composition
Nrg1tm1Leth/Nrg1tm1Leth
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrg1tm1Leth mutation (0 available); any Nrg1 mutation (56 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• severly impaired formation; lack of intertrabecular sinusiods was noted
• less contracted appearance in mutant embryos
• dilated common ventricle at E10.5 before septation occurs
• decreased emptying of the common ventricle was observed at E10.5
• depressed contractility was observed
• occasionally displayed

embryo
• arrested at E11.5

muscle
• severly impaired formation; lack of intertrabecular sinusiods was noted
• depressed contractility was observed

nervous system
• the proximal part of the facio-acoustic ganglion complex is abnormal; mean area reduced by 30%
• the petrosal and nodose ganglia appear normal
• affected ganglia appear to have cells that originated in the crainal neural crest and unaffected ganglia appear to have cells that originated in the placode
• the proximal region including the mandibular branch and CNS projection is missing
• total area of the ganglion is reduced by 66%
• disruption of cellular organization, vacuolization and karyorrhexis was seen
• compromised projections to the brain stem
• compromised projections to the brain stem


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
01/28/2026
MGI 6.24
The Jackson Laboratory