All Phenotypes S1pr3<tm1b(EUCOMM)Wtsi> MGI Mouse

About Help FAQ

Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

S1pr3^{tm1b(EUCOMM)Wtsi}
targeted mutation 1b, Wellcome Trust Sanger Institute
MGI:5636967

Summary

1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	S1pr3^{tm1b(EUCOMM)Wtsi}/S1pr3^{tm1b(EUCOMM)Wtsi}	C57BL/6N-S1pr3^{tm1b(EUCOMM)Wtsi}/Bay	MGI:6263414

Allelic Composition	S1pr3^{tm1b(EUCOMM)Wtsi}/S1pr3^{tm1b(EUCOMM)Wtsi}
Genetic Background	C57BL/6N-S1pr3^{tm1b(EUCOMM)Wtsi}/Bay
Cell Lines	EPD0617_4_E04

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
S1pr3^{tm1b(EUCOMM)Wtsi} mutation (0 available); any S1pr3 mutation (24 available)

Data Sources

IMPC Data for S1pr3

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

cardiovascular system

abnormal retina blood vessel morphology ( J:211773 )

IMPC - BCM

integument

abnormal skin coloration ( J:211773 )

IMPC - BCM

reproductive system

female infertility ( J:211773 )

IMPC - BCM

male infertility ( J:211773 )

IMPC - BCM

vision/eye

abnormal retina morphology ( J:211773 )

IMPC - BCM

abnormal retina blood vessel morphology ( J:211773 )

IMPC - BCM

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 12/10/2024 MGI 6.24