Wdr35 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Wdr35
WD repeat domain 35
MGI:1921932

15 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Wdr35^{tm2a(EUCOMM)Hmgu}/Wdr35^yeti involves: C57BL/6N	abnormal embryo development	J:171617
	absent ribs	J:171617
	impaired somite development	J:171617
	polysyndactyly	J:171617
	short ribs	J:171617
Wdr35^yeti/Wdr35^yeti Not Specified	abnormal direction of embryo turning	J:171617
	abnormal direction of heart looping	J:171617
	abnormal heart tube morphology	J:171617
	absent embryonic cilia	J:171617
	absent ribs	J:171617
	delayed embryo turning	J:171617
	diaphragmatic hernia	J:171617
	edema	J:171617
	embryonic lethality during organogenesis, complete penetrance	J:171617
	impaired somite development	J:171617
	polysyndactyly	J:171617
	pulmonary hypoplasia	J:171617
	tracheoesophageal fistula	J:171617

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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