Gene Gene information from NCBI Gene database.
Entrez ID 65078
Gene name Reticulon 4 receptor
Gene symbol RTN4R
Synonyms (NCBI Gene)
NGRNOGOR
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
miRNA miRNA information provided by mirtarbase database.
64
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
59
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 IBA
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605566 18601 ENSG00000040608
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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 associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
11
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
RTN4R-related disorder Likely benign; Uncertain significance rs144464748, rs117955118, rs149052299, rs1309033080, rs1370988148, rs145150796, rs149231717, rs374126911 RCV003981609
RCV003893877
RCV003912144
RCV003951960
RCV003949509
RCV003924255
RCV003934348
RCV003979183
Schizophrenia Uncertain significance rs779384862 RCV003990901
Schizophrenia, susceptibility to risk factor rs74315508, rs74315509 RCV000005158
RCV000005159
Associations from Text MiningDisease associations identified through Pubtator
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