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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Klc1
kinesin light chain 1
MGI:107978
11 phenotypes from 2 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Klc1m1Btlr/Klc1m1Btlr
C57BL/6J-Klc1m1Btlr
decreased body weight J:254928
Klc1tm1Gsn/Klc1tm1Gsn
B6.129-Klc1tm1Gsn
abnormal axon morphology J:148380
abnormal axonal transport J:148380
abnormal brain white matter morphology J:148380
abnormal spinal cord white matter morphology J:148380
axon degeneration J:148380
axonal dystrophy J:148380
tau protein deposits J:148380
Klc1tm1Gsn/Klc1tm1Gsn
either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
decreased body size J:57877
impaired coordination J:57877
Klc1tm1Gsn/Klc1tm1Gsn
involves: 129S1/Sv * 129X1/SvJ
abnormal vesicle-mediated transport J:170887

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
04/30/2024
MGI 6.23
The Jackson Laboratory