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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Nrp2
neuropilin 2
MGI:1100492
16 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Chn2tm2.1Alk/Chn2+
Nrp2Gt(GST039)Byg/Nrp2+
involves: 129P2/OlaHsd * C57BL/6 * CD-1 * FVB/N 		abnormal hippocampus development J:186252
Flt4tm1Ali/Flt4+
Nrp2tm1Ddg/Nrp2+
involves: C57BL/6 		abnormal lymphangiogenesis J:156869
prenatal lethality, incomplete penetrance J:156869
skin edema J:156869
Flt4tm1Ali/Flt4+
Nrp2tm1Ddg/Nrp2tm1Ddg
involves: C57BL/6 		abnormal lymphangiogenesis J:156869
Gucy2dtm1Mom/Gucy2dtm1Mom
Nrp2tm1.2Mom/Nrp2tm1.2Mom
involves: 129P2/OlaHsd * C57BL/6J 		abnormal olfactory bulb morphology J:125485
Kdrtm1.1Eia/Kdr+
Nrp2tm1Ddg/Nrp2+
involves: 129P2/OlaHsd * C57BL/6 		normal cardiovascular system phenotype J:156869
Nrp1tm1Ddg/Nrp1tm1Ddg
Nrp2tm1Ddg/Nrp2tm1Ddg
involves: 129P2/OlaHsd 		persistent truncus arteriosus J:95697
Nrp1tm1Ddg/Nrp1tm1Ddg
Nrp2tm1Ddg/Nrp2tm1Ddg
involves: 129P2/OlaHsd * C57BL/6 		increased heart atrium size J:93799
persistent truncus arteriosus J:93799
ventricular septal defect J:93799
Nrp1tm1Hfu/Nrp1+
Nrp2tm1Mkl/Nrp2tm1Mkl
involves: BALB/c * C57BL/6 * CBA 		abnormal dorsal aorta morphology J:75477
abnormal vascular development J:75477
abnormal vitelline vasculature morphology J:75477
embryonic lethality during organogenesis, complete penetrance J:75477
hemorrhage J:75477
Nrp1tm1Hfu/Nrp1tm1Hfu
Nrp2tm1Mkl/Nrp2+
involves: BALB/c * C57BL/6 * CBA 		abnormal dorsal aorta morphology J:75477
abnormal vascular development J:75477
abnormal vitelline vasculature morphology J:75477
decreased embryo size J:75477
embryonic lethality during organogenesis, complete penetrance J:75477
hemorrhage J:75477
Nrp1tm2Ddg/Nrp1tm2Ddg
Nrp2tm1Ddg/Nrp2tm1Ddg
Tg(Prrx1-cre)1Cjt/0
involves: 129 * C57BL/6J * SJL/J 		normal cardiovascular system phenotype J:147285
Nrp2tm1.2Mom/Nrp2+
Sema3ftm1.2Ddg/Sema3f+
involves: 129P2/OlaHsd 		abnormal lymphatic vessel endothelial cell morphology J:226501
Nrp2tm1.2Mom/Nrp2tm1.2Mom
Vmn1r49tm1Mom/Vmn1r49tm1Mom
involves: 129P2/OlaHsd * C57BL/6J 		abnormal olfactory bulb morphology J:125485
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory