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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gnao1tm1Ejne
targeted mutation 1, E J Neer
MGI:2152683
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gnao1tm1Ejne/Gnao1tm1Ejne involves: 129S4/SvJae * C57BL/6 MGI:3615486
ht2
Gnao1tm1Ejne/Gnao1+ involves: 129S4/SvJae MGI:5620506


Genotype
MGI:3615486
hm1
Allelic
Composition
Gnao1tm1Ejne/Gnao1tm1Ejne
Genetic
Background
involves: 129S4/SvJae * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gnao1tm1Ejne mutation (0 available); any Gnao1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes continue to display a progressive decline in postnatal survival after day 25, with the last suvivor dying at day 125
• homozygotes are obtained at a reduced Mendelian frequency immediately after birth (14% vs expected 25%); no significant loss is noted in utero
• homozygotes start dying at day 5 after birth; only 20% survive to day 25

cardiovascular system
• homozygotes exhibit loss of normal muscarinic regulation of cardiac L-type calcium channels in ventricular myocytes, suggesting that cardiac failure may be the cause of limited life span
• however, homozygotes display normal electrocardiograms as well as normal muscarinic regulation of atrial K+ channels

nervous system
• homozygotes display occasional seizures, despite absence of obvious histologic abnormalities in the nervous system
• surprisingly, homozygotes exhibit a grossly intact nervous system despite the fact that the encoded protein constitutes 0.2-0.5% of brain particulate protein and 10% of the nerve growth cone membrane
• however, mutant ventricular myocytes exhibit loss of muscarinic inhibition of the isoproterenol-stimulated L-type ventricular calcium channel; the L-type calcium channel responds normally to isoproterenol, but muscarinic inhibition is abolished

behavior/neurological
• homozygotes exhibit tremors when grasped by the tail
• homozygotes display occasional seizures, despite absence of obvious histologic abnormalities in the nervous system




Genotype
MGI:5620506
ht2
Allelic
Composition
Gnao1tm1Ejne/Gnao1+
Genetic
Background
involves: 129S4/SvJae
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gnao1tm1Ejne mutation (0 available); any Gnao1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mice do not show enhancement in sensitivity to pentylenetetrazol (PTZ) kindling





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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