Symbol Name ID |
Efnb1
ephrin B1 MGI:102708 |
Darker colors indicate more annotations |
Human Phenotypes | Sensorineural hearing impairment |
Disease(s) Associated with EFNB1 | |
craniofrontonasal syndrome |
Mouse Phenotypes | abnormal tympanic ring morphology |
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Availability | Mouse Genotype | |
Efnb1tm1.1Sor/Efnb1tm1.1Sor | ||
Efnb1tm1.1Sor/Y | ||
Efnb1tm1Sor/Efnb1+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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 |
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