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DUP2Q31.1 Chromosome 2q31.1 duplication syndrome [ Homo sapiens (human) ]

Gene ID: 100529099, updated on 31-Aug-2024

Summary

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Official Symbol
DUP2Q31.1provided by HGNC
Official Full Name
Chromosome 2q31.1 duplication syndromeprovided by HGNC
Primary source
MIM:613681
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
C2DUPq31.1

Genomic context

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Location:
2q31.1

Bibliography

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Related articles in PubMed

  1. Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes. Sandholm N, et al. J Am Soc Nephrol, 2013 Oct. PMID 24029427, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
Chromosome 2q31.1 duplication syndrome
OMIM: 613681GeneReviews: Not available

General gene information

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Property

  • phenotype only

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