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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Kif1a
kinesin family member 1A
MGI:108391
21 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Kif1algdg-2J/Kif1algdg-2J
C57BL/6J-Kif1algdg-2J/CxJ
hindlimb paralysis J:229662
Kif1algdg/Kif1algdg
C3.Cg-Kif1algdg/GrsrJ
abnormal limb posture J:229662
abnormal locomotor coordination J:229662
decreased body size J:229662
hindlimb paralysis J:229662
increased or absent threshold for auditory brainstem response J:229662
prenatal lethality, incomplete penetrance J:229662
Kif1atm1Noh/Kif1atm1Noh
involves: 129S4/SvJae * C57BL/6
abnormal motor coordination/balance J:47170
abnormal nervous system physiology J:47170
abnormal synaptic vesicle clustering J:47170
abnormal synaptic vesicle number J:47170
ataxia J:47170
axon degeneration J:47170
decreased birth body size J:47170
decreased birth weight J:47170
decreased locomotor activity J:47170
hyporesponsive to tactile stimuli J:47170
impaired balance J:47170
neonatal lethality, incomplete penetrance J:47170
neuron degeneration J:47170
postnatal lethality, complete penetrance J:47170
unresponsive to tactile stimuli J:47170

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
04/16/2024
MGI 6.23
The Jackson Laboratory