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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Npntem1Zhwe/Npntem1Zhwe
C57BL/6-Npntem1Zhwe
abnormal kidney development J:314482
absent kidney J:314482
absent ureter J:314482
perinatal lethality, complete penetrance J:314482
Npnttm1.1Lfr/Npnt+
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
single kidney J:122519
Npnttm1.1Lfr/Npnttm1.1Lfr
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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory