Kif21b Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Kif21b
kinesin family member 21B
MGI:109234

11 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Kif21b^{tm1a(KOMP)Wtsi}/Kif21b^{tm1a(KOMP)Wtsi} C57BL/6N-Kif21b^{tm1a(KOMP)Wtsi}/Wtsi	decreased circulating alanine transaminase level	J:175295
	decreased circulating aspartate transaminase level	J:175295
	decreased circulating serum albumin level	J:175295
	decreased circulating total protein level	J:175295
Kif21b^{tm2a(KOMP)Wtsi}/Kif21b^{tm2a(KOMP)Wtsi} C57BL/6N-Kif21b^{tm2a(KOMP)Wtsi}	abnormal dendrite morphology	J:235389
	abnormal hippocampal pyramidal neuron dendrite morphology	J:235389
	abnormal synapse morphology	J:235389
	normal behavior/neurological phenotype	J:235389
	decreased dendritic spine density	J:235389
	impaired cued conditioning behavior	J:235389
	impaired spatial learning	J:235389

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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