About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
S1pr3+
wild type
MGI:2437824
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cx1
S1pr3tm1Jch/S1pr3+
S1pr2tm1Jch/S1pr2tm1Jch
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N MGI:3700733


Genotype
MGI:3700733
cx1
Allelic
Composition
S1pr3tm1Jch/S1pr3+
S1pr2tm1Jch/S1pr2tm1Jch
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
S1pr2tm1Jch mutation (1 available); any S1pr2 mutation (46 available)
S1pr3tm1Jch mutation (0 available); any S1pr3 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• as early as 4 weeks of age, all mutant mice homozygous for Edg5tm1Jch and heterozygous for Edg3tm1Jch completely lack a startle reflex to acoustic stimuli >90-100 dB





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
06/12/2024
MGI 6.13
The Jackson Laboratory