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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ephb2
Eph receptor B2
MGI:99611
30 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Efnb2tm1Henk/Efnb2+
Ephb2tm2Paw/Ephb2tm2Paw
either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)
hypospadia J:91491
Efnb2tm1Henk/Efnb2+
Ephb2tm2Paw/Ephb2tm2Paw
Ephb3tm1Kln/Ephb3+
either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)
hypospadia J:91491
Efnb2tm1Henk/Efnb2+
Ephb2tm1Paw/Ephb2+
involves: 129S1/Sv * 129X1/SvJ * CD-1
circling J:116671
Ephb1tm1.1Meg/Ephb1tm1.1Meg
Ephb2tm1.1Meg/Ephb2tm1.1Meg
Ephb3tm1.1Meg/Ephb3tm1.1Meg
involves: 129S4/SvJae * C57BL/6
abnormal axon extension J:197489
decreased corpus callosum size J:197489
normal nervous system phenotype J:197489
Ephb1tm1Cmn/Ephb1tm1Cmn
Ephb2tm1Paw/Ephb2+
involves: 129S1/Sv * 129X1/SvJ
abnormal axon morphology J:176056
Ephb1tm1Cmn/Ephb1tm1Cmn
Ephb2tm1Paw/Ephb2tm1Paw
involves: 129S1/Sv * 129X1/SvJ
abnormal axon morphology J:176056
Ephb1tm1Cmn/Ephb1tm1Cmn
Ephb2tm1Paw/Ephb2tm1Paw
involves: 129S1/Sv * 129X1/SvJ * CD-1
abnormal axon morphology J:150550
abnormal axon pruning J:150550
Ephb1tm1Cmn/Ephb1tm1Cmn
Ephb2tm1Paw/Ephb2tm1Paw
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129/Sv * CD-1
abnormal eye morphology J:85573
abnormal optic tract morphology J:85573
Ephb1tm1Cmn/Ephb1tm1Cmn
Ephb2tm1Paw/Ephb2tm1Paw
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ * CD-1
abnormal axon morphology J:150550
abnormal axon pruning J:150550
Ephb1tm1Cmn/Ephb1tm1Cmn
Ephb2tm2Paw/Ephb2+
involves: 129S1/Sv * 129X1/SvJ
abnormal axon morphology J:176056
Ephb1tm1Cmn/Ephb1tm1Cmn
Ephb2tm2Paw/Ephb2tm2Paw
involves: 129S1/Sv * 129X1/SvJ
abnormal axon morphology J:176056
Ephb2tm1Paw/Ephb2+
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ
abnormal axon morphology J:176056
Ephb2tm1Paw/Ephb2+
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ * CD-1
circling J:62565
Ephb2tm1Paw/Ephb2tm1Paw
Ephb3tm1Kln/Ephb3tm1Kln
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)
abnormal anogenital distance J:91491
hypospadia J:91491
Ephb2tm1Paw/Ephb2tm1Paw
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ
abnormal axon morphology J:176056
omphalocele J:173636
Ephb2tm1Paw/Ephb2tm1Paw
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ * CD-1
abnormal axon guidance J:62565
abnormal endolymph J:116671
abnormal inner ear vestibule morphology J:62565
abnormal large intestine crypts of Lieberkuhn morphology J:115873
abnormal Paneth cell morphology J:115873
abnormal semicircular canal morphology J:62565
abnormal sensory neuron innervation pattern J:62565
abnormal vestibular dark cell morphology J:62565
abnormal vestibular endolymph J:116671
abnormal vestibular endolymph ionic homeostasis J:116671
abnormal vestibular system physiology J:62565
circling J:62565
cleft palate J:173636
delayed axon extension J:62565
premature death J:62565
small endolymphatic duct J:62565
Ephb2tm2.1Jf/Ephb2+
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ
abnormal axon morphology J:176056
Ephb2tm2.1Jf/Ephb2tm2.1Jf
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ
abnormal axon morphology J:176056
Ephb2tm2.1Jf/Ephb2tm2.1Jf
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ * CD-1
normal digestive/alimentary phenotype J:157019
Ephb2tm2Paw/Ephb2+
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ * CD-1
circling J:62565
Ephb2tm2Paw/Ephb2tm2Paw
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ
omphalocele J:173636
Ephb2tm2Paw/Ephb2tm2Paw
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ * CD-1
abnormal axon guidance J:62565
abnormal digestive system physiology J:157019
abnormal endolymph J:116671
abnormal large intestine crypts of Lieberkuhn morphology J:115873
abnormal Paneth cell morphology J:115873
abnormal semicircular canal morphology J:62565
abnormal sensory neuron innervation pattern J:62565
abnormal vestibular endolymph J:116671
abnormal vestibular endolymph ionic homeostasis J:116671
abnormal vestibular system physiology J:62565
circling J:62565
cleft palate J:173636
delayed axon extension J:62565
ectopic Paneth cells J:157019
premature death J:62565
small endolymphatic duct J:62565
Ephb2tm3.1Jf/Ephb2tm3.1Jf
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * CD-1
abnormal small intestinal crypt cell proliferation J:157019
normal digestive/alimentary phenotype J:157019
Ephb2tm4.1Jf/Ephb2+
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ
abnormal axon morphology J:176056
Ephb2tm4.1Jf/Ephb2tm4.1Jf
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * CD-1
abnormal digestive system physiology J:157019
normal digestive/alimentary phenotype J:157019
Ephb2tm4.1Jf/Ephb2tm4.1Jf
Ephb3tm1Kln/Ephb3tm1Kln
involves: 129S1/Sv * 129X1/SvJ
abnormal axon morphology J:176056

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
02/11/2020
MGI 6.14
The Jackson Laboratory