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FLASH GENE
Symbol NRG1 contributors: mct/shn - updated : 03-08-2015
HGNC name neuregulin 1
HGNC id 7997
ASSOCIATED DISORDERS
corresponding disease(s) SCZD6
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional fusion      
chimeric protein gamma heregulin (ERBG) by fusion with STIP1 (5'-STIP1-NRG1-3') in translocation t(8;11) (p12;q13
constitutional     --low  
in amyotrophic lateral sclerosis and Parkinson's disease, in cerebral fluid
constitutional     --over  
in Alzheimer's disease
tumoral        
silenced by methylation in breast cancers
Susceptibility
  • to schizophrenia (
  • to late onset Alzheimer's disease with psychoses
  • to Hirschsprung's disease
  • Variant & Polymorphism SNP
  • increasing the risk of late onset Alzheimer's disease families with psychoses
  • SNP increasing the risk of schizophrenia
  • interaction between variants in NRG1 and ERBB4 might contribute to susceptibility for schizophrenia
  • SNP increasing the risk of Hirschsprung's disease
  • Candidate gene
    Marker
    Therapy target
    SystemTypeDisorderPubmed
    cardiovascularaquiredheart failure
    potential use of NRG1s as novel therapy for heart failure
    respiratorylung 
    may represent a novel therapeutic target for mucus hypersecretion in respiratory diseases
    ANIMAL & CELL MODELS
  • in cysteine-rich domain-NRG-1-/-mice, peripheral projections defasciculated and displayed aberrant branching patterns within their targets (
  • knock-down of nrg1 caused near total loss of olig2-positive cerebellar neurones, but caused no apparent loss of spinal motor neurones (
  • misexpression of human NRG1 type III in zebrafish transgenic embryos results in ectopic Schwann cell migration, allowing them to aberrantly enter the central nervous system
  • in murine juvenile testes Ra and Fsh induced meiosis indirectly through Sertoli cells when Nrg1 and Nrg3 were upregulated, as Nrg1 amplified itself and Nrg3