Plexin-B1

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

Plexin-B1 is a protein of the plexin family that in humans is encoded by the PLXNB1 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesPLXNB1, PLEXIN-B1, PLXN5, SEP, plexin B1
Quick facts PLXNB1, Available structures ...
PLXNB1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPLXNB1, PLEXIN-B1, PLXN5, SEP, plexin B1
External IDsOMIM: 601053; MGI: 2154238; HomoloGene: 130508; GeneCards: PLXNB1; OMA:PLXNB1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001130082
NM_002673

NM_172775

RefSeq (protein)

NP_001123554
NP_002664

NP_766363

Location (UCSC)Chr 3: 48.4 – 48.43 MbChr 9: 108.92 – 108.95 Mb
PubMed search[3][4]
Wikidata
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Function

Within neural tissues, the plexin family serves as transmembrane receptors for Semaphorins.[8] Outside of neural tissues, Plexin B1 is implicated in the control of cell migration.[9]

Interactions

PLXNB1 has been shown to interact with ARHGEF12,[10] Rnd1[11] and ARHGEF11.[10][11][12][13]

References

Further reading

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