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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Rnf13
ring finger protein 13
MGI:1346341
9 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Rnf13tm1.1(KOMP)Vlcg/Rnf13tm1.1(KOMP)Vlcg
C57BL/6N-Rnf13tm1.1(KOMP)Vlcg/J
abnormal hindlimb morphology J:211773
abnormal limb position J:211773
abnormal sleep behavior J:211773
increased mean corpuscular hemoglobin J:211773
Rnf13tm1.1Xgao/Rnf13tm1.1Xgao
B6.Cg-Rnf13tm1.1Xgao
abnormal excitatory synapse morphology J:344668
abnormal spatial learning J:344668
abnormal synaptic bouton morphology J:344668
impaired spatial working memory J:344668
increased anxiety-related response J:344668

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
12/10/2024
MGI 6.24
The Jackson Laboratory