All Phenotypes 4931406C07Rik<tm1b(EUCOMM)Wtsi> MGI Mouse

About Help FAQ

Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

4931406C07Rik^{tm1b(EUCOMM)Wtsi}
targeted mutation 1b, Wellcome Trust Sanger Institute
MGI:5637051

Summary

1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	4931406C07Rik^{tm1b(EUCOMM)Wtsi}/4931406C07Rik^{tm1b(EUCOMM)Wtsi}	C57BL/6N-4931406C07Rik^{tm1b(EUCOMM)Wtsi}/BayMmucd	MGI:6696639

Allelic Composition	4931406C07Rik^{tm1b(EUCOMM)Wtsi}/4931406C07Rik^{tm1b(EUCOMM)Wtsi}
Genetic Background	C57BL/6N-4931406C07Rik^{tm1b(EUCOMM)Wtsi}/BayMmucd
Cell Lines	EPD0592_1_H01

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
4931406C07Rik^{tm1b(EUCOMM)Wtsi} mutation (0 available); any 4931406C07Rik mutation (17 available)

Data Sources

IMPC Data for 4931406C07Rik

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

cardiovascular system

increased heart rate variability ( J:211773 )

IMPC - BCM

vision/eye

abnormal eye anterior chamber depth ( J:211773 )

IMPC - BCM

abnormal retina inner nuclear layer 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 11/12/2024 MGI 6.24