GO curators for mouse genes have assigned the following annotations to the gene product of Sema5a. (This text reflects annotations as of Wednesday, January 23, 2013.) Summary from NCBI RefSeq
[Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene belongs to the semaphorin gene family that encodes membrane proteins containing a semaphorin domain and several thrombospondin type-1 repeats. Members of this family are involved in axonal guidance during neural development. This gene has been implicated as an autism susceptibility gene.[provided by RefSeq, Jan 2010]Summary text based on GO annotations supported by experimental evidence in mouse
Researchers have inferred from direct assay, that the gene product of Sema5a
participates in the following biological processes:
Fiore R et al. (2005) Inactivation of the Sema5a gene results in embryonic lethality and defective remodeling of the cranial vascular system. Mol Cell Biol, 25:2310-9. (PubMed:15743826)
Oster SF et al. (2003) Invariant Sema5A inhibition serves an ensheathing function during optic nerve development. Development, 130:775-84. (PubMed:12506007)