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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
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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)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory