Wnt2b Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Wnt2b
wingless-type MMTV integration site family, member 2B
MGI:1261834

8 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Wnt2b^tm1.1Eem/Wnt2b^tm1.1Eem involves: 129X1/SvJ * C57BL/6	no abnormal phenotype detected	J:153098
Wnt2b^{tm1b(EUCOMM)Wtsi}/Wnt2b^{tm1b(EUCOMM)Wtsi} C57BL/6N-Wnt2b^{tm1b(EUCOMM)Wtsi}/Tcp	abnormal kidney morphology	J:211773
	abnormal spleen morphology	J:211773
	enlarged kidney	J:211773
	enlarged spleen	J:211773
	irregularly shaped pupil	J:211773
	persistence of hyaloid vascular system	J:211773
	small spleen	J:211773

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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