About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Krd
kidney and retinal defects
MGI:99258
18 phenotypes from 1 allele in 1 genetic background
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Krd/Krd+
involves: C3H/He * C57BL/6 * YBR/Ki
abnormal eye electrophysiology J:20807
abnormal kidney corticomedullary boundary morphology J:20807
abnormal nephrogenic zone morphology J:20807
abnormal retina layer morphology J:20807
absent kidney J:20807
decreased kidney weight J:20807
decreased nephron number J:20807
delayed kidney development J:20807
dilated ureter J:20807
disorganized retina layers J:20807
kidney cortex hypoplasia J:20807
kidney cyst J:20807
postnatal lethality J:20807
single kidney J:20807
slow postnatal weight gain J:20807
thin retina inner nuclear layer J:20807
thin retina outer nuclear layer J:20807
Krd/Krd
involves: C3H/He * C57BL/6 * YBR/Ki
embryonic lethality at implantation, complete penetrance J:20807

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
05/07/2024
MGI 6.23
The Jackson Laboratory