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: 12234
    Symptom: Symmetrical peromelic reduction of the upper limbs (missing distal, mesial and proximal elements) and symmetrical phocomelic reduction of the lower limbs(missing proximal and mesial elements) without other major malformations
    Reference Information
    PubMed ID: 19996735
    Authors: Harewood L,Keeling JW,Fantes JA,Opitz JM,FitzPatrick DR
    Journal: Clinical dysmorphology
    Related Event(s):
    Event ID: 11424
    Precision: C
    Chromosome Rearrangement Type: Reciprocal Translocation
    Chromosome: 2, 12
    Karyotype: t(2;12)(p25.1;q23.3)
    Breakpoints Information:
    First Breakpoint:
    Location: p25.1
    Second Breakpoint:
    Location: q23.3
    Junction Sequence is Unavailable.
    Experimental Method: FISH