About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3522323
Allelic
Composition
Per1tm1Brd/Per1tm1Brd
Per2tm1Brd/Per2tm1Brd
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Per1tm1Brd mutation (0 available); any Per1 mutation (62 available)
Per2tm1Brd mutation (1 available); any Per2 mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• double homozygotes entrain to the LD cycle (12 h light/12 h dark); normal entrainment is caused by the inhibitory ("masking") effect of light on locomotor activity
• when placed in DD, double homozygotes show no circadian rhythms in locomotor activity, clock, or clock-controlled gene expression
• upon loss of rhythmicity, a light pulse fails to reestablish the circadian rhythm, indicating total absence of a functional clock


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory