Neuregulin 3

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NRG3
Identifiers
AliasesNRG3, HRG3, pro-neuregulin 3
External IDsOMIM: 605533 MGI: 1097165 HomoloGene: 32051 GeneCards: NRG3
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001190187
NM_001190188
NM_008734

RefSeq (protein)

NP_001177116
NP_001177117
NP_032760

Location (UCSC)Chr 10: 81.88 – 82.99 MbChr 14: 38.09 – 39.2 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Neuregulin 3 also known as NRG3 is a member of the neuregulin protein family which in humans is encoded by the NRG3 gene.[5][6]

Function

NRG3 can bind to the extracellular domain of the ERBB4 receptor tyrosine kinase but not to the related family members ERBB2 or ERBB3. NRG3 binding stimulates tyrosine phosphorylation of ERBB4.[6]

Clinical significance

Variants of the NRG3 gene have been linked to a susceptibility to schizophrenia.[7]

It has also been linked to Hirschsprung's disease.[8]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000185737Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000041014Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: NRG3 neuregulin 3".
  6. ^ a b Zhang D, Sliwkowski MX, Mark M, Frantz G, Akita R, Sun Y, Hillan K, Crowley C, Brush J, Godowski PJ (September 1997). "Neuregulin-3 (NRG3): a novel neural tissue-enriched protein that binds and activates ErbB4". Proc. Natl. Acad. Sci. U.S.A. 94 (18): 9562–7. doi:10.1073/pnas.94.18.9562. PMC 23218. PMID 9275162.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  7. ^ Chen PL, Avramopoulos D, Lasseter VK, McGrath JA, Fallin MD, Liang KY, Nestadt G, Feng N, Steel G, Cutting AS, Wolyniec P, Pulver AE, Valle D (January 2009). "Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia". Am. J. Hum. Genet. 84 (1): 21–34. doi:10.1016/j.ajhg.2008.12.00. PMC 2668048. PMID 19118813. {{cite journal}}: Unknown parameter |laysource= ignored (help); Unknown parameter |laysummary= ignored (help)CS1 maint: multiple names: authors list (link)
  8. ^ Yang J, Duan S, Zhong R, Yin J, Pu J, Ke J, Lu X, Zou L, Zhang H, Zhu Z, Wang D, Xiao H, Guo A, Xia J, Miao X, Tang S, Wang G (January 2013). "Exome Sequencing Identified NRG3 as a Novel Susceptible Gene of Hirschsprung's Disease in a Chinese Population". Mol. Neurobiol. 47: 957–966. doi:10.1007/s12035-012-8392-4. PMID 23315268.{{cite journal}}: CS1 maint: multiple names: authors list (link)

Further reading