PLXNC1 (plexin C1)
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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10154 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Plexin C1 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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PLXNC1 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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CD232, PLXN-C1, VESPR |
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Chromosome
Chromosome number
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12 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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12q22 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the plexin family. Plexins are transmembrane receptors for semaphorins, a large family of proteins that regulate axon guidance, cell motility and migration, and the immune response. The encoded protein and its ligand regulate |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | ||||||||||||||||||||||||||
| UniProt ID | O60486 | |||||||||||||||||||||||||
| Protein name | Plexin-C1 (Virus-encoded semaphorin protein receptor) (CD antigen CD232) | |||||||||||||||||||||||||
| Protein function | Receptor for SEMA7A, for smallpox semaphorin A39R, vaccinia virus semaphorin A39R and for herpesvirus Sema protein. Binding of semaphorins triggers cellular responses leading to the rearrangement of the cytoskeleton and to secretion of IL6 and I | |||||||||||||||||||||||||
| PDB | 3KUZ , 3NVN , 3NVQ , 6VXK | |||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Detected in heart, brain, lung, spleen and placenta. {ECO:0000269|PubMed:9586637}. | |||||||||||||||||||||||||
| Sequence |
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| Sequence length | 1568 | |||||||||||||||||||||||||
| Interactions | View interactions | |||||||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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