Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
65078
Gene name Gene Name - the full gene name approved by the HGNC.
Reticulon 4 receptor
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RTN4R
Synonyms (NCBI Gene) Gene synonyms aliases
NGR, NOGOR
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q11.21
Summary Summary of gene provided in NCBI Entrez Gene.
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
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT491729 hsa-miR-3186-5p PAR-CLIP 23592263
MIRT491728 hsa-miR-6820-5p PAR-CLIP 23592263
MIRT491727 hsa-miR-4767 PAR-CLIP 23592263
MIRT491726 hsa-miR-1908-5p PAR-CLIP 23592263
MIRT491725 hsa-miR-663a PAR-CLIP 23592263
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 20463223, 20697954, 32296183
GO:0005783 Component Endoplasmic reticulum IDA
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane ISS
GO:0007166 Process Cell surface receptor signaling pathway ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605566 18601 ENSG00000040608
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

Accession ID Position in sequence Description Type
PF13855 LRR_8 114 166 Leucine rich repeat Repeat
PF13855 LRR_8 156 214 Leucine rich repeat Repeat
PF13855 LRR_8 203 261 Leucine rich repeat Repeat
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
MKRASAGGSRLLAWVLWLQAWQVAAPCPGACVCYNEPKVTTSCPQQGLQAVPVGIPAASQ
RIFLHGNRISHVPAASFRACRNLTILWLHSNVLARIDAAAFTGLALLEQLDLSDNAQLRS
VDPATFHGLGRLHTLHLDRCGLQELGPGLFRGLAA
LQYLYLQDNALQALPDDTFRDLGNL
THLFLHGNRISSVPERAFRGLHSLDRLLLHQNRVAHVHPHAFRDLGRLMTLYLFANNLSA
LPTEALAPLRALQYLRLNDNP
WVCDCRARPLWAWLQKFRGSSSEVPCSLPQRLAGRDLKR
LAANDLQGCAVATGPYHPIWTGRATDEEPLGLPKCCQPDAADKASVLEPGRPASAGNALK
GRVPPGDSPPGNGSGPRHINDSPFGTLPGSAEPPLTAVRPEGSEPPGFPTSGPRRRPGCS
RKNRTRSHCRLGQAGSGGGGTGDSEGSGALPSLTCSLTPLGLALVLWTVLGPC
Sequence length 473
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Axonal growth inhibition (RHOA activation)
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
15532024, 28892071, 19052207
Associations from Text Mining
Disease Name Relationship Type References
Autism Spectrum Disorder Associate 28892071
Bipolar Disorder Associate 27112568
Brain Neoplasms Associate 31649250
Developmental Disabilities Associate 28892071
Diabetes Mellitus Type 2 Associate 36357677
DiGeorge Syndrome Associate 24321711
Glioblastoma Associate 31649250
Glioma Associate 15312170, 31649250
Glucose Intolerance Associate 36357677
Leukemia Myeloid Acute Associate 28965123