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: 10390
    Disease: Bipolar Affective Disorder ( DOID: 10028 )
    Reference Information
    PubMed ID: 11511928
    Authors: Willett-Brozick JE,Savul SA,Richey LE,Baysal BE
    Journal: Human genetics
    Related Event(s):
    Event ID: 10005
    Precision: A
    Chromosome: 9
    Karyotype: ins(9)(p24.2)
    Breakpoints Information:
    Breakpoint:
    Location: p24.2
    Exact position: Chr9: 3615592
    This breakpoint occurs in an intergenic region
    Insertion Source is 12S mitochondrial DNA (mtDNA) between nucleotides 896 and 936 of the mtDNA sequencing.
    Breakpoint is Unavailable
    Experimental Method: PCR, DNA sequencing
    Related Event(s):
    Event ID: 10278
    Precision: A
    Chromosome Rearrangement Type: Reciprocal Translocation
    Chromosome: 9, 11
    Karyotype: t(9;11)(p24;q23)
    Breakpoints Information:
    First Breakpoint:
    Location: p24.2
    Exact position: Chr9: 3615592
    This breakpoint occurs in an intergenic region
    Second Breakpoint:
    Location: q23.1
    Exact position: Chr9: 11172169