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Symbol
Name
ID

Efnb1
ephrin B1
MGI:102708

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
!	Indicates phenotype varies with strain background.
	Darker colors indicate more annotations

Human Phenotypes	Microcephaly	Agenesis of corpus callosum	Hypoplasia of the corpus callosum	Intellectual disability	Global developmental delay
Disease(s) Associated with EFNB1
craniofrontonasal syndrome

Mouse Phenotypes		nervous system phenotype	abnormal corpus callosum morphology	absent corpus callosum	abnormal axon morphology	abnormal cranial ganglia morphology	abnormal oculomotor nerve morphology
Availability	Mouse Genotype	nervous system phenotype	abnormal corpus callosum morphology	absent corpus callosum	abnormal axon morphology	abnormal cranial ganglia morphology	abnormal oculomotor nerve morphology
	Efnb1^tm1.1Sor/Efnb1^tm1.1Sor			!
	Efnb1^tm2.2Sor/Efnb1^tm2.2Sor	*
	Efnb1^tm3.2Sor/Efnb1^tm3.2Sor	*		!
	Efnb1^tm4.2Sor/Efnb1^tm4.2Sor	*
	Efnb1^tm1.1Sor/Efnb1⁺	*!
	Efnb1^tm3.2Sor/Efnb1⁺	*
	Efnb1^tm4.2Sor/Efnb1⁺
	Efnb1^tm1.1Sor/Y			!
	Efnb1^tm2.2Sor/Y	*
	Efnb1^tm3.2Sor/Y	*		!
	Efnb1^tm4.2Sor/Y	*

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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