Npnt Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Npnt
nephronectin
MGI:2148811

9 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Npnt^em1Zhwe/Npnt^em1Zhwe C57BL/6-Npnt^em1Zhwe	abnormal kidney development	J:314482
	absent kidney	J:314482
	absent ureter	J:314482
	perinatal lethality, complete penetrance	J:314482
Npnt^tm1.1Lfr/Npnt⁺ involves: 129P2/OlaHsd * C57BL/6 * FVB/N	single kidney	J:122519
Npnt^tm1.1Lfr/Npnt^tm1.1Lfr involves: 129P2/OlaHsd * C57BL/6 * FVB/N	abnormal kidney development	J:122519
	abnormal kidney morphology	J:122519
	absent kidney	J:122519
	impaired branching involved in ureteric bud morphogenesis	J:122519
	normal renal/urinary system phenotype	J:122519
	small kidney	J:122519

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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