RTN4R (reticulon 4 receptor)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 65078 |
| Gene name | Reticulon 4 receptor |
| Gene symbol | RTN4R |
| Synonyms (NCBI Gene) |
NGRNOGOR
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| Chromosome | 22 |
| Chromosome location | 22q11.21 |
| Summary | 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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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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 from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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