PLXNB1
Sign in to saveAlso known as PLEXIN-B1, PLXN5, SEP, plexin B1
Plexin-B1 is a protein of the plexin family that in humans is encoded by the PLXNB1 gene.
In the Vinony graph
Within Vinony's link graph, PLXNB1 is referenced by 8 other articles, and connects out to Q180686, human chromosome 3 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 3.
Its subject is documented across 6 Wikipedia language editions.
Gene data
PLXNB1- Name
- plexin B1
- Type
- protein-coding
- Position
- 48,401,712–48,430,499 (−)
- Aliases
- PLEXIN-B1, PLXN5, SEP
- Ensembl
- ENSG00000164050
- RefSeq RNA
- NM_001130082.3, NM_002673.6, XM_011533833.3, XM_011533834.2, XM_011533835.2
- RefSeq protein
- NP_001123554.1, NP_002664.2, XP_011532135.1, XP_011532136.1, XP_011532137.1
Enables semaphorin receptor activity. Involved in several processes, including negative regulation of cell adhesion; regulation of cell shape; and semaphorin-plexin signaling pathway. Is integral component of plasma membrane. Part of semaphorin receptor complex. [provided by Alliance of Genome Resources, Apr 2022]
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
plexin B1
- Symbol
- PLXNB1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 3:48,401,712-48,430,499
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Image
- Protein PLXNB1 PDB 2JPH.png
Show 5 more facts
- HomoloGene ID
- 130508
- exact match
- identifiers.org/ncbigene/5364
- genomic end
- 48430086
- genomic start
- 48445261
- cytogenetic location
- 3p21.31
Sources (4)
via Wikidata · CC0
~1 min read
Encyclopedic overview
5 sectionsContents
- Function
- Interactions
- References
- Further reading
- External links
Plexin-B1 is a protein of the plexin family that in humans is encoded by the PLXNB1 gene.
== Function ==
Excerpted from Wikipedia’s “PLXNB1” article, available under the CC BY-SA 4.0 licence.