Ephrin B1
Protein found in humans
From Wikipedia, the free encyclopedia
Ephrin B1 is a protein that in humans is encoded by the EFNB1 gene.[5][6] It is a member of the ephrin family. The encoded protein is a type I membrane protein and a ligand of Eph-related receptor tyrosine kinases. It may play a role in cell adhesion and function in the development or maintenance of the nervous system.[7]
External IDsOMIM: 300035; MGI: 102708; HomoloGene: 3263; GeneCards: EFNB1; OMA:EFNB1 - orthologs
Clinical significance
Mutations in this protein are responsible for most cases of craniofrontonasal syndrome.[8][9][10]