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.
Gene data
PLXNB1- Name
- plexin B1
- Type
- protein-coding
- Aliases
- PLEXIN-B1, PLXN5, SEP
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]
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
View on Ensembl →
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
Article
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 ==
Connections
Q180686
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human chromosome 3
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Ensembl genome database project
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protein
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Wikidata
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gene
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chromosome
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digital object identifier
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bibcode
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human genome
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Q229883
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base pair
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locus
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gene expression
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Online Mendelian Inheritance in Man
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Protein Data Bank
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Q22908627
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Entrez
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Q905695
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Gene Ontology
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