Kif1a Phenotype Annotations

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

Allelic Composition Genetic Background	Annotated Term	Reference
Kif1a^lgdg-2J/Kif1a^lgdg-2J C57BL/6J-Kif1a^lgdg-2J/CxJ	hindlimb paralysis	J:229662
Kif1a^lgdg/Kif1a^lgdg C3.Cg-Kif1a^lgdg/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
Kif1a^tm1Noh/Kif1a^tm1Noh 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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