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: 11005 ( Case ID: 12288 )
    Disease: Diffuse Esophageal Leiomyomatosis ( DOID: 8675 )
    Event Information
    Precision: A
    Chromosome Rearrangement Type: Deletion
    Chromosome: X
    Karyotype: del(x)(q22q22)
    Breakpoints Information:
    First Breakpoint:
    Location: q22
    Exact position: ChrX: 125598450bp
    This breakpoint occurs in intron1 of NM_033381.1.
    Second Breakpoint:
    Location: q22
    Exact position: ChrX: 107677568bp
    This breakpoint occurs in intron2 of NM_033641.2.
    Length of Deletion Segment is 17Kb.
    Junction Sequence :
    The Junction Sequence is Inferred.
    Note: Green and Blue color indicate 5' and 3' sequence according to the breakpoint.
    Experimental Method: FISH, Southern blot, PCR, DNA sequencing
    Reference Information
    PubMed ID: 9463311
    Authors: Ueki Y,Naito I,Oohashi T,Sugimoto M,Seki T,Yoshioka H,Sado Y,Sato H,Sawai T,Sasaki F,Matsuoka M,Fukuda S,Ninomiya Y
    Journal: American journal of human genetics
    Go to Genome Browser ( Click the image )