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: 10317 ( Case ID: 11826 )
    Symptom: Short stature, mild mental retardation, behavioral problems, decreased range of motion of elbows, wrist and fingers, increased tone, and characteristic facial features, attention deficit hyperactivity disorder, Asperger syndrome
    Event Information
    Precision: C
    Chromosome Rearrangement Type: Duplication
    Chromosome: 15
    Karyotype: dup(15)(q24)
    Breakpoints Information:
    First Breakpoint:
    Location: q24
    Second Breakpoint:
    Location: q24
    Length of Duplication Segment is 2.62Mb.
    Junction Sequence is Unavailable.
    Experimental Method: FISH
    Reference Information
    PubMed ID: 19557438
    Authors: El-Hattab AW,Smolarek TA,Walker ME,Schorry EK,Immken LL,Patel G,Abbott MA,Lanpher BC,Ou Z,Kang SH,Patel A,Scaglia F,Lupski JR,Cheung SW,Stankiewicz P
    Journal: Human genetics
    Go to Genome Browser ( Click the image )