About dbCRID

  • dbCRID (Database of Chromosomal Rearrangements In Diseases) is the largest database of curated database of human Chromosome rearrangements and associated diseases.
  • Current release: v 0.9 (06/30/2010).
  • Please direct questions and comments to dbCRID@biolead.org.
  • Related Databases

  • AtlasGeneticsOncology, Atlas of Genetics and Cytogenetics in Oncology and Haematology
  • ChimerDB 2.0, A knowledgebase for fusion genes updated
  • CytoD 1.0, A database of cytogenetic abnormalities.
  • DACRO, A disease-Associated Chromosomal Rearrangements Online.
  • Decipher, , A Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
  • HYBRIDdb,A database of hybrid genes in the human genome.
  • Mitelman, A database of Chromosome Aberrations and Gene Fusions in Cancer.
  • SKY/M-FISH &CGH, A public platform for investigators to share and compare their molecular cytogenetic data.
  • TICdb, A database of Translocation breakpoints In Cancer.
  • References

  • Kong F, Zhu J, Wu J, Peng J, Wang Y, Wang Q, Fu S, Yuan L and Li T: dbCRID: a database of chromosomal rearrangements in human diseases. Nucleic Acids Res. [PubMed] [Full-text]
  • Case ID: 11645
    Disease: Atrial Septal Defect ( DOID: 1882 ) All events related to this disease.
    Reference Information
    PubMed ID: 18179900
    Authors: Kim HG,Kishikawa S,Higgins AW,Seong IS,Donovan DJ,Shen Y,Lally E,Weiss LA,Najm J,Kutsche K,Descartes M,Holt L,Braddock S,Troxell R,Kaplan L,Volkmar F,Klin A,Tsatsanis K,Harris DJ,Noens I,Pauls DL,Daly MJ,MacDonald ME,Morton CC,Quade BJ,Gusella JF
    Journal: American journal of human genetics
    Related Event(s):
    Event ID: 10037
    Precision: C
    Chromosome: 16
    Karyotype: ins(16;2) (q22.1;p16.1p16.3)
    Breakpoints Information:
    Breakpoint:
    Location: q22.1
    Insertion Source is chromosome 2 p16.1p16.3.
    Breakpoint is Unavailable
    Experimental Method: G Banding, FISH