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: 10873
    Symptom: Choroideremia, mild sensorineural deafness, and primary amenorrhea
    Reference Information
    PubMed ID: 11035551
    Authors: Lorda-Sanchez IJ,IbaƱez AJ,Sanz RJ,Trujillo MJ,Anabitarte ME,Querejeta ME,Rodriguez de Alba M,Gimenez A,Infantes F,Ramos C,Garcia-Sandoval B,Ayuso C
    Journal: Ophthalmic genetics
    Related Event(s):
    Event ID: 10591
    Precision: C
    Chromosome Rearrangement Type: Reciprocal Translocation
    Chromosome: X, 4
    Karyotype: t(X ;4(q21.2;p16.3)
    Breakpoints Information:
    First Breakpoint:
    Location: q21.2
    Second Breakpoint:
    Location: p16.3
    Junction Sequence is Unavailable.
    Experimental Method: G Banding, Dual co-hybridzation