Ephb2 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ephb2
Eph receptor B2
MGI:99611

30 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Efnb2^tm1Henk/Efnb2⁺ Ephb2^tm2Paw/Ephb2^tm2Paw either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)	hypospadia	J:91491
Efnb2^tm1Henk/Efnb2⁺ Ephb2^tm2Paw/Ephb2^tm2Paw Ephb3^tm1Kln/Ephb3⁺ either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)	hypospadia	J:91491
Efnb2^tm1Henk/Efnb2⁺ Ephb2^tm1Paw/Ephb2⁺ involves: 129S1/Sv * 129X1/SvJ * CD-1	circling	J:116671
Ephb1^tm1.1Meg/Ephb1^tm1.1Meg Ephb2^tm1.1Meg/Ephb2^tm1.1Meg Ephb3^tm1.1Meg/Ephb3^tm1.1Meg involves: 129S4/SvJae * C57BL/6	abnormal axon extension	J:197489
	decreased corpus callosum size	J:197489
	normal nervous system phenotype	J:197489
Ephb1^tm1Cmn/Ephb1^tm1Cmn Ephb2^tm1Paw/Ephb2⁺ involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:176056
Ephb1^tm1Cmn/Ephb1^tm1Cmn Ephb2^tm1Paw/Ephb2^tm1Paw involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:176056
Ephb1^tm1Cmn/Ephb1^tm1Cmn Ephb2^tm1Paw/Ephb2^tm1Paw involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal axon morphology	J:150550
	abnormal axon pruning	J:150550
Ephb1^tm1Cmn/Ephb1^tm1Cmn Ephb2^tm1Paw/Ephb2^tm1Paw Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129/Sv * CD-1	abnormal eye morphology	J:85573
	abnormal optic tract morphology	J:85573
Ephb1^tm1Cmn/Ephb1^tm1Cmn Ephb2^tm1Paw/Ephb2^tm1Paw Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal axon morphology	J:150550
	abnormal axon pruning	J:150550
Ephb1^tm1Cmn/Ephb1^tm1Cmn Ephb2^tm2Paw/Ephb2⁺ involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:176056
Ephb1^tm1Cmn/Ephb1^tm1Cmn Ephb2^tm2Paw/Ephb2^tm2Paw involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:176056
Ephb2^tm1Paw/Ephb2⁺ Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:176056
Ephb2^tm1Paw/Ephb2⁺ Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ * CD-1	circling	J:62565
Ephb2^tm1Paw/Ephb2^tm1Paw Ephb3^tm1Kln/Ephb3^tm1Kln 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
Ephb2^tm1Paw/Ephb2^tm1Paw Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:176056
	omphalocele	J:173636
Ephb2^tm1Paw/Ephb2^tm1Paw Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal axon guidance	J:62565
	abnormal endolymph physiology	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 ionic homeostasis	J:116671
	abnormal vestibular endolymph physiology	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
Ephb2^tm2.1Jf/Ephb2⁺ Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:176056
Ephb2^tm2.1Jf/Ephb2^tm2.1Jf Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:176056
Ephb2^tm2.1Jf/Ephb2^tm2.1Jf Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ * CD-1	normal digestive/alimentary phenotype	J:157019
Ephb2^tm2Paw/Ephb2⁺ Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ * CD-1	circling	J:62565
Ephb2^tm2Paw/Ephb2^tm2Paw Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ	omphalocele	J:173636
Ephb2^tm2Paw/Ephb2^tm2Paw Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal axon guidance	J:62565
	abnormal digestive system physiology	J:157019
	abnormal endolymph physiology	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 ionic homeostasis	J:116671
	abnormal vestibular endolymph physiology	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
Ephb2^tm3.1Jf/Ephb2^tm3.1Jf Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * CD-1	abnormal small intestinal crypt cell proliferation	J:157019
	normal digestive/alimentary phenotype	J:157019
Ephb2^tm4.1Jf/Ephb2⁺ Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:176056
Ephb2^tm4.1Jf/Ephb2^tm4.1Jf Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * CD-1	abnormal digestive system physiology	J:157019
	normal digestive/alimentary phenotype	J:157019
Ephb2^tm4.1Jf/Ephb2^tm4.1Jf Ephb3^tm1Kln/Ephb3^tm1Kln involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:176056

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