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Symbol
Name
ID
Efnb1
ephrin B1
MGI:102708
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Sensorineural hearing impairment
Disease(s) Associated with EFNB1
craniofrontonasal syndrome

Mouse Phenotypes
abnormal tympanic ring morphology
Availability Mouse Genotype
Efnb1tm1.1Sor/Efnb1tm1.1Sor
Efnb1tm1.1Sor/Y
Efnb1tm1Sor/Efnb1+
H2az2Tg(Wnt1-cre)11Rth/H2az2+  (conditional)

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
04/23/2024
MGI 6.23
The Jackson Laboratory