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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Plxnb2
plexin B2
MGI:2154239
20 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Pax8tm1.1(cre)Mbu/Pax8+
Plxnb1tm1Rkun/Plxnb1tm1Rkun
Plxnb2tm1.1Rkun/Plxnb2tm1.1Rkun
involves: 129P2/OlaHsd * C57BL/6 		abnormal renal tubule epithelium morphology J:221423
Plxnb1tm1.1Ltam/Plxnb1+
Plxnb2tm1Matl/Plxnb2+
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 		normal mortality/aging J:168399
reduced fertility J:168399
Plxnb1tm1.1Ltam/Plxnb1+
Plxnb2tm1Matl/Plxnb2tm1Matl
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 		embryonic lethality J:168399
Plxnb1tm1.1Ltam/Plxnb1tm1.1Ltam
Plxnb2tm1Matl/Plxnb2+
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 		normal mortality/aging J:168399
reduced fertility J:168399
Plxnb1tm1.1Ltam/Plxnb1tm1.1Ltam
Plxnb2tm1Matl/Plxnb2tm1Matl
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 		abnormal ureteric bud trunk morphology J:168399
embryonic lethality J:168399
renal hypoplasia J:168399
Plxnb1tm1Matl/Plxnb1tm1Matl
Plxnb2tm1c(EUCOMM)Wtsi/Plxnb2tm1Matl
Tg(Nes-cre)1Kln/0
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * C57BL/6N * SJL 		abnormal cerebellar lobule formation J:228347
abnormal cerebral cortex morphology J:228347
abnormal cortical ventricular zone morphology J:228347
absent corpus callosum J:228347
decreased corpus callosum size J:228347
decreased neuronal precursor cell number J:228347
decreased neuronal precursor proliferation J:228347
ectopic cerebellar granule cells J:228347
enlarged lateral ventricles J:228347
normal nervous system phenotype J:228347
premature neuronal precursor differentiation J:228347
thin cerebral cortex J:228347
Plxnb2tm1Matl/Plxnb2+
Sema4ctm1Matl/Sema4ctm1Matl
B6.129P2-Sema4ctm1Matl Plxnb2tm1Matl 		abnormal cerebellar granule layer morphology J:167973
Plxnb2tm1Matl/Plxnb2+
Sema4gtm1Kik/Sema4gtm1Kik
B6.Cg-Plxnb2tm1Matl Sema4gtm1Kik 		normal nervous system phenotype J:167973
Plxnb2tm1Matl/Plxnb2tm1Matl
Sema4ctm1Matl/Sema4ctm1Matl
B6.129P2-Sema4ctm1Matl Plxnb2tm1Matl 		abnormal cerebellar granule cell migration J:167973
abnormal cerebellar granule layer morphology J:167973
Plxnb2tm1Matl/Plxnb2tm1Matl
Sema4gtm1Kik/Sema4gtm1Kik
B6.Cg-Plxnb2tm1Matl Sema4gtm1Kik 		abnormal cerebellar granule cell migration J:167973
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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
04/09/2024
MGI 6.23 		The Jackson Laboratory