RTN4 - reticulon 4 Gene

Also Known as ASY; NSP; NOGO; RTN-X; NSP-CL; RTN4-A; RTN4-C; RTN4-B1; RTN4-B2; NI220/250; Nbla00271; Nbla10545

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 57142

About RTN4

Cytogenetic location: 2p16.1 Genomic coordinates (GRCh38): 2:54,972,189-55,137,831 (from NCBI)

This gene has 14 transcripts (splice variants), 221 orthologues and 4 paralogues. Ubiquitous expression in fat (RPKM 122.1), brain (RPKM 104.7) and 24 other tissues.

Summary

This gene belongs to the family of reticulon encoding genes. Reticulons are associated with the endoplasmic reticulum, and are involved in neuroendocrine secretion or in membrane trafficking in neuroendocrine cells. The product of this gene is a potent neurite outgrowth inhibitor which may also help block the regeneration of the central nervous system in higher vertebrates. Alternatively spliced transcript variants derived both from differential splicing and differential promoter usage and encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

RTN4 Products (11)

mRNA Protein Name
NM_001321859.2 NP_001308788.1 reticulon-4 isoform E
NM_001321860.1 NP_001308789.1 reticulon-4 isoform E
NM_001321861.2 NP_001308790.1 reticulon-4 isoform E
NM_001321862.2 NP_001308791.1 reticulon-4 isoform E
NM_001321863.2 NP_001308792.1 reticulon-4 isoform E
NM_001321904.2 NP_001308833.1 reticulon-4 isoform E
NM_007008.3 NP_008939.1 reticulon-4 isoform C
NM_020532.5 NP_065393.1 reticulon-4 isoform A
NM_153828.3 NP_722550.1 reticulon-4 isoform B
NM_207520.2 NP_997403.1 reticulon-4 isoform D
NM_207521.2 NP_997404.1 reticulon-4 isoform E
Molecular Function GO Annotation Evidence References Source
enables cadherin binding IPI
IPI: Inferred from physical interaction
21183689 GOA
enables metal ion binding EXP
EXP: Inferred from Experiment
15317586 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11126360 GOA
enables protein homodimerization activity IDA
IDA: Inferred from direct assay
27786289 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
27353365 GOA
Biological Process GO Annotation Evidence References Source
involved in cell adhesion involved in sprouting angiogenesis IDA
IDA: Inferred from direct assay
15034570 GOA
involved in endoplasmic reticulum organization IDA
IDA: Inferred from direct assay
27786289 GOA
involved in endoplasmic reticulum tubular network formation IDA
IDA: Inferred from direct assay
24262037 GOA
involved in endoplasmic reticulum tubular network membrane organization IMP
IMP: Inferred from mutant phenotype
27619977 GOA
involved in endoplasmic reticulum tubular network organization IMP
IMP: Inferred from mutant phenotype
18779370 GOA
involved in negative regulation of amyloid-beta formation IDA
IDA: Inferred from direct assay
15286784 GOA
involved in negative regulation of axon extension IDA
IDA: Inferred from direct assay
10667797 GOA
involved in negative regulation of cell growth IMP
IMP: Inferred from mutant phenotype
20463223 GOA
involved in nuclear pore complex assembly IMP
IMP: Inferred from mutant phenotype
26906412 GOA
involved in positive regulation of ERBB3 signaling pathway IMP
IMP: Inferred from mutant phenotype
27353365 GOA
involved in positive regulation of epithelial cell migration IMP
IMP: Inferred from mutant phenotype
27353365 GOA
involved in positive regulation of mammary gland epithelial cell proliferation IMP
IMP: Inferred from mutant phenotype
27353365 GOA
involved in positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction IMP
IMP: Inferred from mutant phenotype
27353365 GOA
involved in positive regulation of protein localization to endoplasmic reticulum IDA
IDA: Inferred from direct assay
27353365 GOA
involved in protein stabilization IMP
IMP: Inferred from mutant phenotype
27353365 GOA
acts upstream of or within regulation of cell migration IDA
IDA: Inferred from direct assay
15034570 GOA
Cellular Component GO Annotation Evidence References Source
located in cell junction IDA
IDA: Inferred from direct assay
21183689 GOA
located in endoplasmic reticulum membrane IDA
IDA: Inferred from direct assay
10667797 GOA
located in endoplasmic reticulum tubular network IDA
IDA: Inferred from direct assay
27353365 GOA
located in endoplasmic reticulum tubular network membrane IDA
IDA: Inferred from direct assay
27619977 GOA
located in nuclear envelope IDA
IDA: Inferred from direct assay
11126360 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
15034570 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

RTN4 Protein Structure

Reticulon

Reticulon: Reticulon (1005 - 1174)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1192 a.a.
Protein Preferred Names Protein Names

reticulon-4

  • Human NogoA

RTN4 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
RTN4 Q9NQC3 SYT16 Homo sapiens Q17RD7 29892012
Intra
RTN4 Q9NQC3 SYT16 Homo sapiens Q17RD7 31515488
Intra
RTN4 Q9NQC3 SYT16 Homo sapiens Q17RD7 25416956
Intra
RTN4 Q9NQC3 SYT16 Homo sapiens Q17RD7 25416956
Intra
RTN4 Q9NQC3 RTN2 Homo sapiens O75298 35271311
Intra
RTN4 Q9NQC3 RTN2 Homo sapiens O75298 33961781
Intra
RTN4 Q9NQC3 SNX1 Homo sapiens Q13596 25416956
Intra
RTN4 Q9NQC3 ZFYVE21 Homo sapiens Q9BQ24 25416956
Intra
RTN4 Q9NQC3 ARL6IP1 Homo sapiens Q15041 33961781
Intra
RTN4 Q9NQC3 ARL6IP1 Homo sapiens Q15041 25416956
Intra
RTN4 Q9NQC3 SNX15 Homo sapiens Q9NRS6 25416956
Intra
RTN4 Q9NQC3 SNX15 Homo sapiens Q9NRS6 25416956
Intra
RTN4 Q9NQC3 CERT1 Homo sapiens Q9Y5P4 29892012
Intra
RTN4 Q9NQC3 CERT1 Homo sapiens Q9Y5P4 31515488
Intra
RTN4 Q9NQC3 RTN3 Homo sapiens O95197 35271311
Cross: Cross-species interaction Intra: Intraspecies interaction

RTN4 Antibodies

Cat. No. Product Name Application Reactivity
HY-P81675 Nogo Antibody (YA1420) WB, IHC-P, ICC/IF, FC, IP Human

Related Diseases

Diseases Alias
Temporal Lobe Epilepsy
  • Epilepsy, Temporal Lobe

  • Epilepsy Temporal Lobe

Oligodendroglioma
  • Oligodendroglial Neoplasm

  • Oligodendroglial Tumor

  • Oligodendroglial Tumors

  • Well Differentiated Oligodendroglioma

Anosognosia
Optic Atrophy 10 With Or Without Ataxia, Mental Retardation, And Seizures
  • OPA10

  • Optic Atrophy 10 With Or Without Ataxia, Intellectual Disability, And Seizures

  • Optic Atrophy 10

  • Atrophy, Optic, Type 10, With/Without Ataxia, Mental Retardation, And Seizures

Amyotrophic Lateral Sclerosis 1
  • Amyotrophic Lateral Sclerosis

  • ALS

  • Lou Gehrig Disease

  • Amyotrophic Lateral Sclerosis Type 1

  • Charcot Disease

  • ALS1

  • Amyotrophic Lateral Sclerosis, Susceptibility To

  • Fals

  • Lou Gehrig'S Disease

  • Mnd

  • Motor Neuron Disease

  • Familial Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis 1, Familial

  • Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

  • Motor Neuron Disease, Bulbar

  • Motor Neurone Disease

  • Amyotrophic Lateral Sclerosis With Dementia

  • Dementia With Amyotrophic Lateral Sclerosis

  • Motor Neuron Disease, Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic

  • Sclerosis, Lateral, Amyotrophic, Type 1

  • Amyotrophic Sclerosis

  • Als - [Amyotrophic Lateral Sclerosis]

  • Wasting Palsy

  • Amyotrophic Paralysis

  • Amyotrophy Lateral Sclerosis

  • Wasting Paralysis

  • Spinal Progressive Amyotrophy

  • Progressive Atrophic Paralysis

Multiple Sclerosis
  • MS

  • Multiple Sclerosis, Susceptibility To

  • Disseminated Sclerosis

  • Multiple Sclerosis, Disease Progression, Modifier Of

  • Insular Sclerosis

  • Multiple Sclerosis Modifier Of Disease Progression

  • Multiple Sclerosis, Susceptibility To 1

  • Multiple Sclerosis, Susceptibility To, 1

  • Multiple Sclerosis 1

  • Generalized Multiple Sclerosis

  • Multiple Sclerosis Variant

  • Multiple Sclerosis Susceptibility To

  • Cerebrospinal Sclerosis

  • Generalised Multiple Sclerosis

  • Ms - [Multiple Sclerosis]

  • Disseminated Cerebrospinal Sclerosis

  • Disseminated Multiple Sclerosis

  • Disseminated Nervous System Myelosclerosis

  • Multiple Cerebrospinal Sclerosis

  • Multiple Combined Sclerosis

  • Multiple Sclerosis Generalised

  • Disseminated Brain Sclerosis

  • Disseminated Spinal Sclerosis

  • Insular Brain Sclerosis

  • Miliary Brain Sclerosis

  • Multiple Combined Sclerosis Of Spinal Cord

  • Multiple Ascending Sclerosis

  • Multiple Brain Sclerosis

  • Multiple Sclerosis Of Brain Stem

  • Multiple Sclerosis Of The Brain Stem

  • Multiple Sclerosis Of Cord

  • Sclérose En Plaques

  • Plaque Sclerosis

  • Multiple Sclerosis Of The Spinal Cord

Cholestasis, Intrahepatic, Of Pregnancy 3
  • ICP3

  • Cholestasis, Intrahepatic, Of Pregnancy, 3

  • Intrahepatic Cholestasis Of Pregnancy 3

  • Pregnancy Related Cholestasis 3

  • Cholestasis Of Pregnancy, Intrahepatic 3

  • Cholestasis, Intrahepatic, Of Pregnancy, Type 3

Neuropathy, Hereditary Sensory And Autonomic, Type Iia
  • Hereditary Sensory And Autonomic Neuropathy Type 2

  • Hsan2

  • HSAN2A

  • Morvan Disease

  • Hereditary Sensory And Autonomic Neuropathy Type Ii

  • Neurogenic Acroosteolysis

  • Hsan Iia

  • Hsn2a

  • Hsn Iia

  • Neuropathy, Progressive Sensory, Of Children

  • Neuropathy, Congenital Sensory

  • Neuropathy, Hereditary Sensory And Autonomic, Type Ii

  • Hereditary Sensory And Autonomic Neuropathy Type 2a

  • Hereditary Sensory And Autonomic Neuropathy Type Iia

  • Hsanii

  • Congenital Sensory Neuropathy

  • Hsan Type Ii

  • Morvan Syndrome

  • Neuropathy, Hereditary Sensory And Autonomic, Type 2a

  • Morvan'S Disease

  • Neuropathy, Hereditary Sensory, Type Iia

  • Acroosteolysis, Neurogenic

  • Acroosteolysis, Giaccai Type

  • Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive

  • Hereditary Sensory Autonomic Neuropathy Type 2

  • Giaccai Type Acroosteolysis

  • Hereditary Sensory Neuropathy Type 2

  • Hereditary Sensory Radicular Neuropathy, Recessive Form

  • Hsan2b

  • Hsan2c

  • Hsan2d

  • Hsn Type Ii

  • Autosomal Recessive Sensory Radicular Neuropathy

  • Limbic Encephalitis-Neuromyotonia-Hyperhidrosis-Polyneuropathy Syndrome

  • Morvan Fibrillary Chorea

  • Neuropathy, Hereditary Sensory And Autonomic, 2a

  • Acroosteolysis Giaccai Type

  • Hereditary Sensory Neuropathy Type Iia

  • Hereditary Sensory Radicular Neuropathy Autosomal Recessive

  • Progressive Sensory Neuropathy Of Children

  • Neuropathy Congenital Sensory

  • Charcot-Marie-Tooth Disease

  • Neuropathy, Sensory And Autonomic, Hereditary, Type Iia

  • Hereditary Sensory Autonomic Neuropathy, Type 2

  • Hereditary Motor And Sensory-Neuropathy Type Ii

  • Sensory Neuropathy, Hereditary

  • Neuropathy, Hereditary Sensory And Autonomic, Type Iib

Cardiomyopathy, Dilated, 1dd
  • Dilated Cardiomyopathy 1dd

  • CMD1DD

  • Cardiomyopathy, Dilated 1dd

  • Cardiomyopathy, Dilated, Type 1dd

Kleptomania
  • Pathological Stealing

Syringomyelia
  • Hydromyelia

Schizophrenia
  • SCZD

  • Schizophrenia With Or Without An Affective Disorder

  • Schizophrenia 12

  • Schizophrenia, Susceptibility To

  • Schizophrenia-1

  • Dementia Praecox

  • Schizophrenia 1

Osebold-Remondini Syndrome
  • Brachydactyly Type A6

  • Brachymesophalangy With Mesomelic Short Limbs And Carpal And Tarsal Osseous Abnormalities

  • Bda6

  • Brachydactyly, Type A6

Dilated Cardiomyopathy
  • Familial Dilated Cardiomyopathy

  • Primary Dilated Cardiomyopathy

  • Idiopathic Dilated Cardiomyopathy

  • Congestive Cardiomyopathy

  • Idiopathic Dilation Cardiomyopathy

  • Primary Familial Dilated Cardiomyopathy

  • Cardiomyopathy, Dilated

  • DCM

  • Cardiomyopathy, Familial Dilated

  • Dilated Cardiomyopathy, Familial

  • Hypokinetic Dilated Cardiomyopathy, Familial

  • Familial Idiopathic Cardiomyopathy

  • Fdc

  • Cardiomyopathy, Familial Idiopathic

  • Idiopathic Cardiomegaly

  • Dilated Congestive Cardiomyopathy

  • Chronic Dilated Cardiomyopathy

  • Ccm - [Congestive Cardiomyopathy]

  • Cocm - [Congestive Cardiomyopathy]

  • Dcm - [Dilated Cardiomyopathy]

  • Dilated-Hypokinetic Cardiomyopathy

  • Congestive Idiopathic Cardiomyopathy

  • Primary Idiopathic Dilated Cardiomyopathy

Stroke, Ischemic
  • Cerebral Infarction

  • Stroke

  • Ischemic Stroke

  • Cerebrovascular Accident

  • Cerebral Infarction, Susceptibility To

  • Stroke, Ischemic, Susceptibility To

  • Cerebral Infarct

  • Ischemic Stroke, Susceptibility To

  • Stroke, Susceptibility To

  • Cva - Cerebral Infarction

  • ISCHSTR

  • Ischemic Cerebrovascular Accident

Attention Deficit-Hyperactivity Disorder
  • Attention Deficit Hyperactivity Disorder

  • ADHD

  • Attention Deficit Disorder

  • Attention Deficit-Hyperactivity Disorder, Susceptibility To

  • Attention Deficit Disorder With Hyperactivity

  • Hyperkinetic Disorder

  • Hyperactivity Of Childhood

  • Attention-Deficit/Hyperactivity Disorder

  • Add

  • Addh

  • Attention Deficit

  • Attention Deficit Disorder Of Childhood With Hyperactivity

  • Attention Deficit Disorder With Hyperactivity Syndrome

  • Hyperkinetic Syndrome

  • Attention-Deficit Hyperactivity Disorder

  • Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type

  • Disturbance Of Activity And Attention

  • Disorder Of Activity And Attention

  • Adhd - [Attention Deficit Hyperactivity Disorder]

  • Hyperkinetic Disorders

  • Disorder Of Activity And Attention With Hyperkinesia

  • Attention Deficit Syndrome With Hyperactivity

Parkinson Disease, Late-Onset
  • Parkinson Disease

  • Parkinson'S Disease

  • PD

  • PARK

  • Parkinson Disease, Susceptibility To

  • Late Onset Parkinson'S Disease

  • Late Onset Parkinson Disease

  • Paralysis Agitans

  • Primary Parkinsonism

  • Idiopathic Parkinson Disease

  • Parkinson'S

  • Parkinson Disease, Late-Onset, Susceptibility To

  • Parkinson Disease, Age Of Onset, Modifier

  • Lewy Body Parkinson Disease

  • Idiopathic Parkinson'S Disease

  • Pd - [Parkinson Disease]

  • Parkinson Disease Nos

  • Parkinson, Nos

  • Primary Parkinson Disease

Alzheimer Disease, Familial, 1
  • Alzheimer Disease

  • Alzheimer'S Disease

  • Presenile And Senile Dementia

  • AD1

  • Alzheimer Disease, Susceptibility To

  • Alzheimer Disease, Late-Onset, Susceptibility To

  • Alzheimer Disease 1, Familial

  • AD

  • Familial Alzheimer Disease

  • Alzheimer Disease, Late-Onset

  • Alzheimers Dementia

  • Alzheimer Dementia

  • Alzheimer Sclerosis

  • Alzheimer Syndrome

  • Alzheimer-Type Dementia

  • Dat

  • Primary Senile Degenerative Dementia

  • Sdat

  • Alzheimer Disease 1

  • Autosomal Dominant Alzheimer Disease

  • Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

  • Late Onset Alzheimer Disease

  • Alzheimers Disease

  • Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

  • Late-Onset Alzheimers Disease

  • Alzheimer'S Disease Pathway Kegg

  • Dementia Due To Alzheimer'S Disease

  • Alzheimer Disease Type 1

  • Alzheimers

Hereditary Spastic Paraplegia
  • Familial Spastic Paraplegia

  • Hereditary Spastic Paraparesis

  • Strumpell-Lorrain Disease

  • Familial Spastic Paraparesis

  • Hsp

  • Spg

  • Strümpell-Lorrain Disease

  • Spastic Paraplegia, Hereditary

  • French Settlement Disease

  • Strumpell-Lorrain Syndrome

  • Fsp

  • Spastic Paraplegia, Familial

  • Spastic Paraplegia Hereditary

  • Spastic Paraplegia 3, Autosomal Dominant

  • Spastic Paraparesis

  • Hereditary Spastic Paralysis

  • Familial Spastic Paralysis

  • Hereditary Spastic Ataxia

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta RTN4 VGNC VGNC:106215
Felis catus RTN4 VGNC VGNC:81215
Bos taurus RTN4 VGNC VGNC:106907
Mus musculus RTN4 MGD MGI:1915835
Rattus norvegicus RTN4 RGD RGD:620989
Canis familiaris RTN4 VGNC VGNC:54541
Others RTN4 NCBI