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Phenotypes Associated with This Genotype
Genotype
MGI:3054890
Allelic
Composition
Rasd1tm1Pngr/Rasd1tm1Pngr
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rasd1tm1Pngr mutation (0 available); any Rasd1 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• circadian period shortened in constant dark
• partially due to spontaneous activity
• restriction of spontaneous activity results in longer circadian period
• premature onset of nocturnal activity
• ability to entrain to low intensity light is diminished or absent


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
03/31/2026
MGI 6.24
The Jackson Laboratory