Clxn Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Clxn
calaxin
MGI:1914043

17 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Clxn^tm1.1Osb/Clxn^tm1.1Osb involves: C57BL * C57BL/6NSlc * DBA	abnormal brain ependyma motile cilium physiology	J:278278
	abnormal left-right axis patterning	J:278278
	abnormal motile primary cilium morphology	J:278278
	abnormal motile primary cilium physiology	J:278278
	abnormal respiratory motile cilium physiology	J:278278
	absent embryonic cilia	J:278278
	asthenozoospermia	J:278278
	cardiac hypertrophy	J:278278
	normal cellular phenotype	J:278278
	decreased embryonic cilium number	J:278278
	decreased litter size	J:278278
	enlarged brain ventricles	J:278278
	enlarged lateral ventricles	J:278278
	hydrocephaly	J:278278
	lethality throughout fetal growth and development, incomplete penetrance	J:278278
	normal reproductive system phenotype	J:278278
	situs inversus	J:278278

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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