2. Gene
  3. NTNG1 - netrin G1 Gene

NTNG1 - netrin G1 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as Lmnt1

Gene ID: 22854 | Gene type: protein coding

About NTNG1

Cytogenetic location: 1p13.3 Genomic coordinates (GRCh38): 1:107,140,088-107,484,923 (from NCBI)

This gene has 10 transcripts (splice variants), 270 orthologues, 27 paralogues and is associated with 2 phenotypes. Broad expression in brain (RPKM 1.0), kidney (RPKM 0.9) and 14 other tissues.

Summary

This gene encodes a preproprotein that is processed into a secreted protein containing eukaroytic growth factor (EGF)-like domains. This protein acts to guide axon growth during neuronal development. Polymorphisms in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Aug 2015]

NTNG1 Products(11)

mRNA Protein Name
NM_001113226.3 NP_001106697.1 netrin-G1 isoform G1a preproprotein
NM_001113228.3 NP_001106699.1 netrin-G1 isoform G1d precursor
NM_001312688.2 NP_001299617.1 netrin-G1 isoform G1n precursor
NM_001330665.2 NP_001317594.1 netrin-G1 isoform 5 precursor
NM_001372166.1 NP_001359095.1 netrin-G1 isoform 6 precursor
NM_001372167.1 NP_001359096.1 netrin-G1 isoform G1a preproprotein
NM_001372168.1 NP_001359097.1 netrin-G1 isoform G1c precursor
NM_001372169.1 NP_001359098.1 netrin-G1 isoform G1d precursor
NM_001372170.1 NP_001359099.1 netrin-G1 isoform G1a preproprotein
NM_001372171.1 NP_001359100.1 netrin-G1 isoform G1c precursor
NM_014917.4 NP_055732.2 netrin-G1 isoform G1c precursor
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables cell adhesion molecule binding IPI
IPI: Inferred from physical interaction
23986473 GOA
enables cell-cell adhesion mediator activity IGI
IGI: Inferred from genetic interaction
23986473 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
14595443 GOA
Biological Process GO Annotation Evidence Reference Source
involved in synaptic membrane adhesion IGI
IGI: Inferred from genetic interaction
23986473 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

NTNG1 Protein Structure

Laminin_N

Laminin_N: Laminin N-terminal (Domain VI) (69 - 295)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (297 - 341)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (364 - 417)

Laminin_EGF

Laminin_EGF: Laminin EGF domain (420 - 457)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 539 a.a.
Protein Preferred Names Protein Names

netrin-G1

axon guidance molecule

Recombinant NTNG1 Proteins

Cat. No. Product Name Accession Purity
HY-P71175 NTNG1 Protein, Human (Biotinylated, HEK293, Avi-His) Q9Y2I2 (H29-S409) ≥95%
HY-P71176 NTNG1 Protein, Human (HEK293, His) Q9Y2I2 (H29-S409) ≥95%

Related Diseases

Diseases Alias
Rett Syndrome

Atypical Rett Syndrome

RTT

Rett Disorder

Rts

Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use

Rett Syndrome, Preserved Speech Variant

Rett Syndrome, Atypical

Rett'S Disorder

Rett Syndrome Variant

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome

Cerebroatrophic Hyperammonemia

Rett Like Syndrome

Rett'S Syndrome

Atypical Rtt

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use

Rett Syndrome Preserved Speech Variant

Rett Syndrome Zappella Variant

Rett Syndrome, Zappella Variant
Non-Specific Syndromic Intellectual Disability

Complex Neurodevelopmental Disorder
Schizophrenia 12

Sczd12

Schizophrenia Susceptibility Locus, Chromosome 1p-Related
Partial Fetal Alcohol Syndrome
St. Louis Encephalitis

Saint Louis Encephalitis

Neuroinvasive St. Louis Encephalitis Virus Infection

Encephalitis, St. Louis

Neuroinvasive Saint Louis Encephalitis Virus Infection

St. Louis Encephalitis Virus Infection

St. Louis Encephalitis Virus Neuroinvasive Disease

St. Louis Viral Disease

Type C Lethargic Encephalitis

Encephalitis Type C
Schizophrenia

SCZD

Schizophrenia With Or Without An Affective Disorder

Schizophrenia 12

Schizophrenia, Susceptibility To

Schizophrenia-1

Dementia Praecox

Schizophrenia 1
Intellectual Developmental Disorder, Autosomal Dominant 41

MRD41

Autosomal Dominant Non-Syndromic Intellectual Disability 41

Mental Retardation, Autosomal Dominant 41

Autosomal Dominant Intellectual Developmental Disorder 41

Autosomal Dominant Mental Retardation 41

Mental Retardation, Autosomal Dominant, Type 41
Glass Syndrome

Chromosome 2q32-Q33 Deletion Syndrome

Satb2-Associated Syndrome

2q33.1 Microdeletion Syndrome

Sas

2q32-Q33 Microdeletion Syndrome

2q32q33 Microdeletion Syndrome

Monosomy 2q32

Monosomy 2q32-Q33

Monosomy 2q32q33

2q32 Deletion Syndrome

Del(2)(Q32)

Del(2)(Q32q33)

GLASS

2q32q33 Microdeletion Syndromes

Satb2 Syndrome

Satb2-Associated Syndrome Due To A Chromosomal Rearrangement

Del(2)(Q33.1)

Monosomy 2q33.1

Satb2-Associated Syndrome Due To A Pathogenic Variant

Satb2-Associated Syndrome Due To A Point Mutation

Satb2 Associated Disorder
Alcohol-Related Birth Defects

Arbd

Alcohol-Related Birth Defect

Alcohol Related Birth Defect

Fetal Alcohol Syndrome
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy

Catecholaminergic Polymorphic Ventricular Tachycardia 1

Ventricular Tachycardia, Catecholaminergic Polymorphic, 1

CPVT1

Ventricular Tachycardia, Stress-Induced Polymorphic

Vtsip

Bidirectional Tachycardia

Stress-Induced Polymorphic Ventricular Tachycardia

Cvpt1

Double Tachycardia Induced By Catecholamines

Malignant Paroxysmal Ventricular Tachycardia

Multifocal Ventricular Premature Beats

Paroxysmal Ventricular Fibrillation

Syncopal Paroxysmal Tachycardia

Syncopal Tachyarythmia

Ventricular Tachycardia Catecholaminergic Polymorphic 1

Tachycardia, Ventricular, Catecholaminergic Polymorphic, Type 1

Multifocal Pvcs

Multifocal Premature Ventricular Beats

Paroxysmal Familial Ventricular Fibrillation

Catecholaminergic Polymorphic Ventricular Tachycardia Type 1
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

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS09625 NTNG1 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Bos taurus NTNG1 VGNC VGNC:50086
Canis familiaris NTNG1 VGNC VGNC:58321
Felis catus NTNG1 VGNC VGNC:63906
Rattus norvegicus NTNG1 RGD RGD:1563465
Mus musculus NTNG1 MGD MGI:1934028
Macaca mulatta NTNG1 VGNC VGNC:75450
Others NTNG1 NCBI