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: 11239 ( Case ID: 11944 )
    Disease: Congenital Cataract ( DOID: 9704 )
    Event Information
    Precision: C
    Chromosome Rearrangement Type: Reciprocal Translocation
    Chromosome: 16, 22
    Karyotype: t(16;22)(p13.3;q11.2)
    Breakpoints Information:
    First Breakpoint:
    Location: p13.3
    Second Breakpoint:
    Location: q11.2
    Junction Sequence is Unavailable.
    Experimental Method: RT-PCR
    Reference Information
    PubMed ID: 17492639
    Authors: Jamieson RV,Farrar N,Stewart K,Perveen R,Mihelec M,Carette M,Grigg JR,McAvoy JW,Lovicu FJ,Tam PP,Scambler P,Lloyd IC,Donnai D,Black GC
    Journal: Human mutation
    Go to Genome Browser ( Click the image )