PLXNB2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Plexin-B2 is a protein that in humans is encoded by the PLXNB2 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesPLXNB2, MM1, Nbla00445, PLEXB2, dJ402G11.3, plexin B2
Quick facts Available structures, PDB ...
PLXNB2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPLXNB2, MM1, Nbla00445, PLEXB2, dJ402G11.3, plexin B2
External IDsOMIM: 604293; MGI: 2154239; HomoloGene: 66630; GeneCards: PLXNB2; OMA:PLXNB2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_012401

NM_001159521
NM_001284506
NM_138749

RefSeq (protein)

NP_001152993
NP_001271435
NP_620088

Location (UCSC)Chr 22: 50.27 – 50.31 MbChr 15: 89.04 – 89.06 Mb
PubMed search[3][4]
Wikidata
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Function

Members of the B class of plexins, such as PLXNB2 are transmembrane receptors that participate in axon guidance and cell migration in response to semaphorins (Perrot et al. (2002)).[supplied by OMIM][7]

Interactions

PLXNB2 has been shown to interact with ARHGEF11.[6][8]

References

Further reading

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