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: 10305 ( Case ID: 11752 )
    Symptom: Moderately severe developmental delay, absence of speech, talipes, congenital dislocation of the hip
    Event Information
    Precision: C
    Chromosome Rearrangement Type: Duplication
    Chromosome: 17
    Karyotype: dup(17)(p12;p10p12)
    Breakpoints Information:
    Insertion Breakpoint:
    Location: p12
    First Breakpoint:
    Location: p10
    Second Breakpoint:
    Location: p12
    Length of Duplication Segment is 9.5Mb.
    Junction Sequence is Unavailable.
    Experimental Method: GTG Banding, FISH
    Reference Information
    PubMed ID: 14699617
    Authors: Shaw CJ,Stankiewicz P,Christodoulou J,Smith E,Jones K,Lupski JR
    Journal: American journal of medical genetics. Part A
    Go to Genome Browser ( Click the image )