RTN4R (reticulon 4 receptor)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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65078 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Reticulon 4 receptor |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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RTN4R |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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NGR, NOGOR |
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Chromosome
Chromosome number
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22 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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22q11.21 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes the receptor for reticulon 4, oligodendrocyte myelin glycoprotein and myelin-associated glycoprotein. This receptor mediates axonal growth inhibition and may play a role in regulating axonal regeneration and plasticity in the adult centr |
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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 | Q9BZR6 | ||||||||||||||||||||
| Protein name | Reticulon-4 receptor (Nogo receptor) (NgR) (Nogo-66 receptor) | ||||||||||||||||||||
| Protein function | Receptor for RTN4, OMG and MAG (PubMed:12037567, PubMed:12068310, PubMed:12089450, PubMed:12426574, PubMed:12839991, PubMed:16712417, PubMed:18411262, PubMed:19052207). Functions as a receptor for the sialylated gangliosides GT1b and GM1 (PubMed | ||||||||||||||||||||
| PDB | 1OZN , 1P8T | ||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Widespread in the brain but highest levels in the gray matter. Low levels in heart and kidney; not expressed in oligodendrocytes (white matter). {ECO:0000269|PubMed:12694398}. | ||||||||||||||||||||
| Sequence |
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| Sequence length | 473 | ||||||||||||||||||||
| 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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