Efnb3 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Efnb3
ephrin B3
MGI:109196

20 phenotypes from 10 alleles in 8 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Efnb3^lltw/Efnb3^lltw C57BL/6J-Efnb3^lltw/GrsrJ	ataxia	J:223790
	normal hearing/vestibular/ear phenotype	J:223790
	impaired righting response	J:223790
	normal mortality/aging	J:223790
	normal vision/eye phenotype	J:223790
Efnb3^lltw/Efnb3^lltw involves: C3H/HeSnJ * C57BL/6J	ataxia	J:223790
	impaired righting response	J:223790
	prenatal lethality, incomplete penetrance	J:223790
Efnb3^m1Btlr/Efnb3^m1Btlr involves: C57BL/6J	abnormal righting response	J:194586
Efnb3^m1Btlr/Efnb3^m1Btlr involves: C57BL/6J	impaired limb coordination	J:194586
Efnb3^tm1.1Henk/Efnb3^tm1.1Henk either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	no abnormal phenotype detected	J:87497
Efnb3^tm1.1Henk/Efnb3^tm1.1Henk involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal axon morphology	J:150550
	abnormal axon pruning	J:150550
Efnb3^tm1.2Henk/Efnb3^tm1.2Henk either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	no abnormal phenotype detected	J:87497
Efnb3^tm1Henk/Efnb3^tm1Henk either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	abnormal corticospinal tract morphology	J:87497
	abnormal gait	J:87497
	abnormal innervation	J:87497
	impaired coordination	J:87497
Efnb3^tm1Henk/Efnb3^tm1Henk involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal axon morphology	J:150550
	abnormal axon pruning	J:150550
Efnb3^tm1Nwg/Efnb3^tm1Nwg involves: 129 * C57BL/6	abnormal long-term depression	J:87398
	normal nervous system phenotype	J:87398
	reduced long-term potentiation	J:87398
Efnb3^tm1Nwg/Efnb3^tm1Nwg involves: C57BL/6	abnormal central pattern generator function	J:82479
	abnormal corticospinal tract morphology	J:82479
	abnormal gait	J:82479
	abnormal motor neuron innervation pattern	J:82479
Efnb3^tm1Nwg/Efnb3^tm1Nwg Not Specified	abnormal corticospinal tract morphology	J:68814
Efnb3^tm1Nwg/Efnb3^tm1Nwg Not Specified	abnormal gait	J:68814
Efnb3^tm2.1Henk/Efnb3^tm2.1Henk involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal axon morphology	J:150550
	abnormal axon pruning	J:150550
Efnb3^tm2Henk/Efnb3^tm2Henk involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal gait	J:150550
Efnb3^tm3.1Henk/Efnb3^tm3.1Henk involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal axon morphology	J:150550
	abnormal axon pruning	J:150550
Efnb3^tm3Henk/Efnb3^tm3Henk involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal gait	J:150550

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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