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: 10147
    Symptom: Microcephaly with closure of the coronary and sagittal suture, cleft palate, hypertelorism
    Reference Information
    PubMed ID: 1433237
    Authors: Van Der Burgt CJ,Merkx GF,Janssen AH,Mulder JC,Suijkerbuijk RF,Smeets DF
    Journal: Journal of medical genetics
    Related Event(s):
    Event ID: 10035
    Precision: C
    Chromosome Rearrangement Type: Deletion
    Chromosome: 5
    Karyotype: del(5)(q34qter)
    Breakpoints Information:
    First Breakpoint:
    Location: q34
    Second Breakpoint:
    Location: qter
    Junction Sequence is Unavailable.
    Experimental Method: G Banding, FISH
    Related Event(s):
    Event ID: 10036
    Precision: C
    Chromosome Rearrangement Type: Deletion
    Chromosome: 16
    Karyotype: del(16)(p11.2pter)
    Breakpoints Information:
    First Breakpoint:
    Location: p11.2
    Second Breakpoint:
    Location: pter
    Junction Sequence is Unavailable.
    Experimental Method: G Banding, FISH
    Related Event(s):
    Event ID: 10037
    Precision: C
    Chromosome Rearrangement Type: Deletion
    Chromosome: 12
    Karyotype: del(12)(q12p13.1)
    Breakpoints Information:
    First Breakpoint:
    Location: q12
    Second Breakpoint:
    Location: p13.1
    Junction Sequence is Unavailable.
    Experimental Method: G Banding, FISH
    Related Event(s):
    Event ID: 10038
    Precision: C
    Chromosome Rearrangement Type: Deletion
    Chromosome: 11
    Karyotype: del(11)(p15.3pter)
    Breakpoints Information:
    First Breakpoint:
    Location: p15.3
    Second Breakpoint:
    Location: pter
    Junction Sequence is Unavailable.
    Experimental Method: G Banding, FISH
    Related Event(s):
    Event ID: 10103
    Precision: C
    Chromosome Rearrangement Type: Reciprocal Translocation
    Chromosome: 11, 12
    Karyotype: t(11;12)(p15;q12)
    Breakpoints Information:
    First Breakpoint:
    Location: p15
    Second Breakpoint:
    Location: q12
    Junction Sequence is Unavailable.
    Experimental Method: FISH
    Related Event(s):
    Event ID: 10104
    Precision: C
    Chromosome Rearrangement Type: Reciprocal Translocation
    Chromosome: 12, 16
    Karyotype: t(12;16)(p13.1 ;p11.2)
    Breakpoints Information:
    First Breakpoint:
    Location: p13.1
    Second Breakpoint:
    Location: p11.2
    Junction Sequence is Unavailable.
    Experimental Method: FISH