| Primary Identifier | MGI:102708 | Organism | mouse, laboratory |
| Chromosome | X | NCBI Gene Number | 13641 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Enables ephrin receptor binding activity. Acts upstream of or within several processes, including axon guidance; neural crest cell migration; and positive regulation of T cell activation. Located in cytoplasm; membrane raft; and nucleus. Is expressed in several structures, including alimentary system; central nervous system; genitourinary system; limb; and sensory organ. Used to study craniofrontonasal syndrome. Human ortholog(s) of this gene implicated in craniofrontonasal syndrome and dysostosis. Orthologous to human EFNB1 (ephrin B1). PHENOTYPE: Engineered alleles of this gene produce cranialfacial defects resulting in neonatal lethality. [provided by MGI curators] |
Features --> Cross References
Canonical gene --> CDSs in specific strains.
Canonical gene --> Exons in specific strains
Canonical gene --> Strain-specific IDs, biotypes, and locations
Canonical gene --> Transcripts in specific strains.
Features --> Overlapping features
