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Open Access Articles- Top Results for MNX1

MNX1

Template:Infobox3cols/rowTemplate:Infobox3cols/rowTemplate:Infobox3cols/rowTemplate:Infobox3cols/row
Identifiers
SymbolsMNX1 ; HB9; HLXB9; HOXHB9; SCRA1
External IDsOMIM142994 MGI109160 HomoloGene21137 GeneCards: MNX1 Gene
RNA expression pattern
File:PBB GE HLXB9 214614 at tn.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez311015285
EnsemblENSG00000130675ENSMUSG00000001566
UniProtP50219Q9QZW9
RefSeq (mRNA)NM_001165255NM_019944
RefSeq (protein)NP_001158727NP_064328
Location (UCSC)Chr 7:
156.79 – 156.8 Mb
Chr 5:
29.47 – 29.48 Mb
PubMed search[1][2]

Motor neuron and pancreas homeobox 1 (MNX1), also known as Homeobox HB9 (HLXB9), is a human protein encoded by the MNX1 gene.[1]

Clinical significance

Mutations in the MNX1 gene are associated with Currarino syndrome.[2]

References

  1. ^ "Entrez Gene: HLXB9 homeobox HB9". 
  2. ^ Merello E, De Marco P, Ravegnani M, Riccipetitoni G, Cama A, Capra V (2013). "Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases". Eur J Med Genet 56 (12): 648–54. PMID 24095820. doi:10.1016/j.ejmg.2013.09.011. 

Further reading

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External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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