Aliases for OLFM2 Gene
Neuronal Olfactomedin Related ER Localized Protein 2 3
Noelin 2 2
External Ids for OLFM2 Gene
Previous GeneCards Identifiers for OLFM2 Gene
OLFM2 (Olfactomedin 2) is a Protein Coding gene.
Diseases associated with OLFM2 include Arteriosclerosis Obliterans.
An important paralog of this gene is OLFM3.
Involved in transforming growth factor beta (TGF-beta)-induced smooth muscle differentiation. TGF-beta induces expression and translocation of OLFM2 to the nucleus where it binds to SRF, causing its dissociation from the transcriptional repressor HEY2/HERP1 and facilitating binding of SRF to target genes (PubMed:25298399). Plays a role in AMPAR complex organization (By similarity). Is a regulator of vascular smooth-muscle cell (SMC) phenotypic switching, that acts by promoting RUNX2 and inhibiting MYOCD binding to SRF. SMC phenotypic switching is the process through which vascular SMCs undergo transition between a quiescent contractile phenotype and a proliferative synthetic phenotype in response to pathological stimuli. SMC phenotypic plasticity is essential for vascular development and remodeling (By similarity).
No data available for
Entrez Gene Summary ,
CIViC summary ,
Tocris Summary ,
PharmGKB "VIP" Summary ,
fRNAdb sequence ontologies and
for OLFM2 Gene