Symbol Name ID

Efnb1 ephrin B1 MGI:102708

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1 matching Allele (1 Gene/Marker represented)

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                       Allele Symbol
Name                         Chr     Synonyms          Category                                                                     Phenotypic Classes                                                                            Human Diseases            

Efnb1tm1.1Sor
ephrin B1; targeted mutation 1.1, Philippe Soriano  X    ephrin-B1null  Targeted (knock-out)  cellular, craniofacial, digestive/alimentary, embryogenesis, hearing/vestibular/ear, integument, limbs/digits/tail, nervous system, skeleton  Craniofrontonasal Syndrome; CFNS 304110