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: 10678 ( Case ID: 11993 )
    Symptom: A progressive asymmetry in the length of his legs,ADHD and impulsive regulation disorder,large hands
    Event Information
    Precision: A
    Chromosome Rearrangement Type: Inversion
    Chromosome: 5
    Karyotype: inv(5)(q15q33.2)
    Breakpoints Information:
    First Breakpoint:
    Location: q15
    Exact position: Chr5: 95102566bp
    This breakpoint occurs in intron 7 of NM_014899.3.
    Second Breakpoint:
    Location: q33.2
    Exact position: Chr5: 154953714bp
    This breakpoint occurs in an intergenic region
    Length of Inversion Segment is 59851148.
    Junction Sequence is Unavailable
    Experimental Method: DNA sequencing
    Reference Information
    PubMed ID: 19953122
    Authors: Chen W,Ullmann R,Langnick C,Menzel C,Wotschofsky Z,Hu H,Döring A,Hu Y,Kang H,Tzschach A,Hoeltzenbein M,Neitzel H,Markus S,Wiedersberg E,Kistner G,van Ravenswaaij-Arts CM,Kleefstra T,Kalscheuer VM,Ropers HH
    Journal: European journal of human genetics : EJHG
    Go to Genome Browser ( Click the image )