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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Kif17
kinesin family member 17
MGI:1098229
9 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Kif17tm1Noh/Kif17tm1Noh
Not Specified
abnormal axonal transport J:174822
abnormal spatial learning J:174822
normal behavior/neurological phenotype J:174822
impaired contextual conditioning behavior J:174822
impaired long-term object recognition memory J:174822
impaired synaptic plasticity J:174822
reduced long-term depression J:174822
reduced long-term potentiation J:174822
reduced NMDA-mediated synaptic currents J:174822

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