MNX1

MNX1
Identifiers
Aliases MNX1, HB9, HLXB9, HOXHB9, SCRA1, motor neuron and pancreas homeobox 1
External IDs MGI: 109160 HomoloGene: 21137 GeneCards: MNX1
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

3110

15285

Ensembl

ENSG00000130675

ENSMUSG00000001566

UniProt

P50219

Q9QZW9

RefSeq (mRNA)

NM_005515
NM_001165255

NM_019944

RefSeq (protein)

NP_001158727.1
NP_005506.3

n/a

Location (UCSC) Chr 7: 156.99 – 157.01 Mb Chr 5: 29.47 – 29.48 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

Motor neuron and pancreas homeobox 1 (MNX1), also known as Homeobox HB9 (HLXB9), is a human protein encoded by the MNX1 gene.[3]

Clinical significance

Mutations in the MNX1 gene are associated with Currarino syndrome.[4]

References

  1. "Human PubMed Reference:".
  2. "Mouse PubMed Reference:".
  3. "Entrez Gene: HLXB9 homeobox HB9".
  4. 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. doi:10.1016/j.ejmg.2013.09.011. PMID 24095820.

Further reading

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


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