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]
  • Event ID: 10777 ( Case ID: 13449 )
    Disease: lung adenocarcinoma ( DOID: 3908 )
    Event Information
    Precision: B
    Chromosome Rearrangement Type: Inversion
    Chromosome: 2
    Karyotype: inv(2)(p21p23)
    Breakpoints Information:
    First Breakpoint:
    Location: p21
    This breakpoint occurs in intron6 of NM_001145076.1.
    Second Breakpoint:
    Location: p23
    This breakpoint occurs in intron19 of NM_004304.3.
    Junction Sequence is Unavailable.
    Experimental Method: FISH, RT-PCR
    Reference Information
    PubMed ID: 18593892
    Authors: Choi YL,Takeuchi K,Soda M,Inamura K,Togashi Y,Hatano S,Enomoto M,Hamada T,Haruta H,Watanabe H,Kurashina K,Hatanaka H,Ueno T,Takada S,Yamashita Y,Sugiyama Y,Ishikawa Y,Mano H
    Journal: Cancer research
    Go to Genome Browser ( Click the image )