PLXNA2

 Plexin-A2 is a protein that in humans is coded by the PLXNA2 gene.[5][6]

PLXNA2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPLXNA2, OCT, PLXN2, plexin A2
External IDsOMIM601054 MGI107684 HomoloGene56427 GeneCardsPLXNA2
Gene location (Human)
Chromosome 1 (human)
Chr.Chromosome 1 (human)[1]
Chromosome 1 (human)
Genomic location for PLXNA2
Genomic location for PLXNA2
Band1q32.2Start208,022,242 bp[1]
End208,244,384 bp[1]
RNA expression pattern
PBB GE PLXNA2 gnf1h09338 s at fs.png

PBB GE PLXNA2 207290 at fs.png

PBB GE PLXNA2 213030 s at fs.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_025179

NM_008882

RefSeq (protein)

NP_079455

NP_032908

Location (UCSC)Chr 1: 208.02 – 208.24 MbChr 1: 194.62 – 194.82 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

This gene encodes a member of the plexin-A family of semaphorin co-receptors. Semaphorins are a large family of secreted or membrane-bound proteins that mediate repulsive effects on axon pathfinding during nervous system development. A subset of semaphorins are recognized by plexin-A/neuropilin transmembrane receptor complexes, triggering a cellular signal transduction cascade that leads to axon repulsion. This plexin-A family member is thought to transduce signals from semaphorin-3A and -3C.[6]

In some studies, the PLXNA2 gene is associated with schizophrenia.[7] and anxiety.[8]

This article uses material from the Wikipedia article
 Metasyntactic variable, which is released under the 
Creative Commons
Attribution-ShareAlike 3.0 Unported License
.