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: 10156
    Disease: Pancreatic Tumours ( DOID: 2891 ) All events related to this disease.
    Reference Information
    PubMed ID: 8494707
    Authors: Bardi G,Johansson B,Pandis N,Mandahl N,Bak-Jensen E,Andrén-Sandberg A,Mitelman F,Heim S
    Journal: British journal of cancer
    Related Event(s):
    Event ID: 10010
    Precision: B
    Chromosome Rearrangement Type: Inversion
    Chromosome: 9
    Karyotype: inv(9) (p1 lp24)
    Breakpoints Information:
    First Breakpoint:
    Location: p21
    Second Breakpoint:
    Location: p24
    Junction Sequence is Unavailable.
    Experimental Method: Karytype analysis
    Related Event(s):
    Event ID: 10112
    Precision: C
    Chromosome Rearrangement Type: Reciprocal Translocation
    Chromosome: 6, 18
    Karyotype: t(6;18)(q21;q21)
    Breakpoints Information:
    First Breakpoint:
    Location: q21
    Second Breakpoint:
    Location: q21
    Junction Sequence is Unavailable.
    Experimental Method: Karytype analysis
    Related Event(s):
    Event ID: 10113
    Precision: C
    Chromosome Rearrangement Type: Reciprocal Translocation
    Chromosome: 6, 19
    Karyotype: t(6;19)(q21;p13)
    Breakpoints Information:
    First Breakpoint:
    Location: q21
    Second Breakpoint:
    Location: p13
    Junction Sequence is Unavailable.
    Experimental Method: Karytype analysis
    Related Event(s):
    Event ID: 10114
    Precision: C
    Chromosome Rearrangement Type: Reciprocal Translocation
    Chromosome: 3, 22
    Karyotype: t(3;22)(q11;p11)
    Breakpoints Information:
    First Breakpoint:
    Location: q11
    Second Breakpoint:
    Location: p11
    Junction Sequence is Unavailable.
    Experimental Method: Karytype analysis