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: 11026
    Symptom: Bilateral aniridia and psychomotor retardation
    Reference Information
    PubMed ID: 16717455
    Authors: Rivera H,Ayala-Madrigal ML,Barros-Núñez JP,Arnaud-López L,Maloney V,Crolla JA
    Journal: Cytogenetic and genome research
    Related Event(s):
    Event ID: 10019
    Precision: C
    Chromosome: 11
    Karyotype: ins(11;11)(p14.1;p13p13)
    Breakpoints Information:
    Breakpoint:
    Location: p14.1
    Insertion Source is chromosome 11 p13p13.
    Breakpoint is Unavailable
    Experimental Method: FISH, G Banding
    Related Event(s):
    Event ID: 10020
    Precision: C
    Chromosome: 11
    Karyotype: ins(11;3)(p11.2;q13.13q13.31)
    Breakpoints Information:
    Breakpoint:
    Location: p11.2
    Insertion Source is chromosome 3 q13.13q13.31.
    Breakpoint is Unavailable
    Experimental Method: FISH, G Banding
    Related Event(s):
    Event ID: 10620
    Precision: C
    Chromosome Rearrangement Type: Inversion
    Chromosome: 11
    Karyotype: inv(11)(p11.2q12)
    Breakpoints Information:
    First Breakpoint:
    Location: p11.2
    Second Breakpoint:
    Location: q12
    Junction Sequence is Unavailable.
    Experimental Method: FISH, G Banding
    Related Event(s):
    Event ID: 10621
    Precision: C
    Chromosome Rearrangement Type: Inversion
    Chromosome: 11
    Karyotype: inv(11)(p13p12)
    Breakpoints Information:
    First Breakpoint:
    Location: p13
    Second Breakpoint:
    Location: p12
    Junction Sequence is Unavailable.
    Experimental Method: FISH, G Banding