NARS1 - asparaginyl-tRNA synthetase 1 Gene

Also Known as NARS; ASNRS; NEDMILG; NEDMILEG

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 4677

About NARS1

Cytogenetic location: 18q21.31 Genomic coordinates (GRCh38): 18:57,600,656-57,621,836 (from NCBI)

This gene has 12 transcripts (splice variants), 233 orthologues, 4 paralogues and is associated with 4 phenotypes. Ubiquitous expression in thyroid (RPKM 64.3), kidney (RPKM 57.0) and 25 other tissues.

Summary

Aminoacyl-tRNA synthetases are a class of Enzymes that charge tRNAs with their cognate Amino acids. Asparaginyl-tRNA synthetase is localized to the cytoplasm and belongs to the class II family of tRNA synthetases. The N-terminal domain represents the signature sequence for the eukaryotic asparaginyl-tRNA synthetases. [provided by RefSeq, Jul 2008]

NARS1 Products (1)

mRNA Protein Name
NM_004539.4 NP_004530.1 asparagine--tRNA ligase, cytoplasmic
Molecular Function GO Annotation Evidence Verweise Source
enables CCR3 chemokine receptor binding IDA
IDA: Inferred from direct assay
30171954 GOA
enables asparagine-tRNA ligase activity IMP
IMP: Inferred from mutant phenotype
9421509 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16713569 GOA
enables protein dimerization activity IDA
IDA: Inferred from direct assay
9421509 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in asparaginyl-tRNA aminoacylation IDA
IDA: Inferred from direct assay
9421509 GOA
involved in cell migration IDA
IDA: Inferred from direct assay
9421509 GOA
involved in cerebral cortex development IMP
IMP: Inferred from mutant phenotype
32788587 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

NARS1 Protein Structure

tRNA_anti-codon

tRNA_anti-codon: OB-fold nucleic acid binding domain (128 - 208)

tRNA-synt_2

tRNA-synt_2: tRNA synthetases class II (D, K and N) (227 - 542)

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

asparagine--tRNA ligase, cytoplasmic

  • asparagine tRNA ligase 1, cytoplasmic

NARS1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
NARS1 O43776 ATXN1 Homo sapiens P54253 32814053
Intra
NARS1 O43776 ATXN1 Homo sapiens P54253 32814053
Intra
NARS1 O43776 ATXN1 Homo sapiens P54253 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant NARS1 Proteins

Art. -Nr. Produktname Accession Reinheit
HY-P74738 NARS Protein, Human (sf9, His) O43776 (M1-P548) ≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Neurodevelopmental Disorder With Microcephaly, Impaired Language, Epilepsy, And Gait Abnormalities
  • NEDMILEG

  • Neurodevelopmental Disorder With Microcephaly, Impaired Language, Epilepsy, And Gait Abnormalities, Autosomal Dominant

Neurodevelopmental Disorder With Microcephaly, Impaired Language, And Gait Abnormalities
  • NEDMILG

  • Neurodevelopmental Disorder With Microcephaly, Impaired Language, And Gait Abnormalities, Autosomal Recessive

Mitochondrial Complex I Deficiency, Nuclear Type 35
  • MC1DN35

  • Mitochondrial Complex 1 Deficiency, Nuclear Type 35

  • Nuclear Type Mitochondrial Complex I Deficiency 35

Myositis
  • Idiopathic Inflammatory Myopathy

  • Idiopathic Inflammatory Myositis

  • Iim

  • Imm

  • Idiopathic Inflammatory Myopathies

  • Myopathy, Familial Idiopathic Inflammatory

  • Inflammatory Disorder Of Muscle

  • Idiopathic Inflammatory Myopathy, Familial

  • Inflammatory Myopathy, Idiopathic

  • Myopathies Idiopathic Inflammatory

  • Familial Idiopathic Inflammatory Myopathy

Interstitial Lung Disease
  • Ild

  • Lung Diseases, Interstitial

  • Lung Diseases Interstitial

  • Interstitial Lung Diseases

Lung Disease
  • Lung Diseases

  • Disorder Of Lung

  • Abnormality Of The Lung

Deafness, Autosomal Recessive 94
  • DFNB94

  • Autosomal Recessive Nonsyndromic Deafness 94

  • Autosomal Recessive Deafness 94

  • Deafness, Autosomal Recessive, 94

Filarial Elephantiasis
  • Lymphatic Filariasis

  • Elephantiasis

  • Filariasis

  • Bancroftian Elephantiasis

  • Bancroftian Filarial Chyluria

  • Elephantiasis Of Eyelid

  • Bancroftian Filariasis

  • Elephantitis

  • Malayi Tropical Eosinphilia

  • Wuchereria Bancrofti Infection

  • Wuchereriasis

  • Elephantiasis, Filarial

  • Filarial Elephantiases

  • Infection By Wuchereria Bancrofti

  • Filarial Lymphangitis

  • Tropical Elephantiasis

  • Filarial Chylocele

Microcephaly
  • Microencephaly

  • Microcephalus

  • Microcephalic

  • Nanocephaly

  • Congenital Microcephaly

  • Brain Hypoplasia

  • Brain Nondevelopment

  • Cephalic Hypoplasia

  • Undeveloped Cerebrum

  • Undeveloped Brain

  • Micrencephalon

  • Micrencephaly

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
Rattus norvegicus NARS1 RGD RGD:1307238
Mus musculus NARS1 MGD MGI:1917473
Felis catus NARS1 VGNC VGNC:68416
Macaca mulatta NARS1 VGNC VGNC:75132
Canis familiaris NARS1 VGNC VGNC:43625
Others NARS1 NCBI