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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gnb3tm1(KOMP)Vlcg
targeted mutation 1, Velocigene
MGI:3812642
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gnb3tm1(KOMP)Vlcg/Gnb3tm1(KOMP)Vlcg involves: C57BL/6NTac MGI:5440450


Genotype
MGI:5440450
hm1
Allelic
Composition
Gnb3tm1(KOMP)Vlcg/Gnb3tm1(KOMP)Vlcg
Genetic
Background
involves: C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gnb3tm1(KOMP)Vlcg mutation (1 available); any Gnb3 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only 10% of mice are alive at 3 weeks of age

vision/eye
• rod bipolar dendrites are not maintained in the invagination of the rod termini
• abnormal rod synaptic tetrad
• in an electroretinogram, mice lack clear positive-going (b) wave and the negative wave starts to rise soon after reaching its peak
• saturated (mixed) conditions, b wave is reduced compared to in wild-type mice
• 2 of 24 retinal cells give a small response to a strong light flash compared with 14 of 25 wild-type cells
• mice exhibit a greater reduction in con-driven b wave than rod-generated b wave
• however, mice exhibit normal negative (a) waves and residual b wave
• saturated cone-generated negative ERG phase rises faster than the photopic a wave in Grm6tm1Nak homozygotes
• however, mice exhibit normal response amplitudes under photopic conditions
• for scotopic conditions, b wave is reduced compared to in wild-type mice

nervous system
• rod bipolar dendrites are not maintained in the invagination of the rod termini
• abnormal rod synaptic tetrad





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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
11/12/2024
MGI 6.24
The Jackson Laboratory