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: 10009 ( Case ID: 11792 )
    Patient Information: A girl
    Symptom: Autism, mental retardation, and mild dysmorphism
    Event Information
    Precision: A
    Chromosome Rearrangement Type: Ring Chromosome
    Chromosome: 17
    Karyotype: r(17)(p13.3q25.3)
    Breakpoints Information:
    First Breakpoint:
    Location: p13.3
    Exact position: Chr17 1944854bp
    This breakpoint occurs in exon11 of NM_001383.3.
    Second Breakpoint:
    Location: q25.3
    Exact position: Chr17 80208921bp
    This breakpoint occurs in intron3 of NM_001893.3.
    Junction Sequence is Unavailable.
    Experimental Method: aCGH, PCR, DNA sequencing
    Reference Information
    PubMed ID: 17996402
    Authors: Vazna A,Havlovicova M,Sedlacek Z
    Journal: Gene
    Go to Genome Browser ( Click the image )