Chromosome 2q31.1 duplication syndrome gene

Genetic element in the species Homo sapiens

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DUP2Q31.1

Identifiers
Aliases| C2DUPq31.1Chromosome 2q31.1 duplication syndrome
External IDs| GeneCards: [1]; OMA:\- orthologs
| Orthologs

Species| Human| Mouse
Entrez| |

100529099

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Ensembl| |

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UniProt| |

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RefSeq (mRNA)| |

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RefSeq (protein)| |

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Location (UCSC)| n/a| n/a
PubMed search| [1]| n/a
Wikidata
| View/Edit Human|

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Chromosome 2q31.1 duplication syndrome is a protein that in humans is encoded by the DUP2Q31.1 gene. [2]

## References

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1. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
2. ^ "Entrez Gene: Chromosome 2q31.1 duplication syndrome". Retrieved 2016-07-25.

## Further reading

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* Sandholm N, McKnight AJ, Salem RM, Brennan EP, Forsblom C, Harjutsalo V, Mäkinen VP, McKay GJ, Sadlier DM, Williams WW, Martin F, Panduru NM, Tarnow L, Tuomilehto J, Tryggvason K, Zerbini G, Comeau ME, Langefeld CD, Godson C, Hirschhorn JN, Maxwell AP, Florez JC, Groop PH (2013). "Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes". J. Am. Soc. Nephrol. 24 (10): 1537–43. doi:10.1681/ASN.2012111122. PMC 3785274. PMID 24029427.

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