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: 10707 ( Case ID: 11286 )
    Symptom: Neonatal hypotonia, normal to accelerated growth, absent to severely delayed speech, global developmental delay, and minor dysmorphic facial features
    Event Information
    Precision: A
    Chromosome Rearrangement Type: Deletion
    Chromosome: 22
    Karyotype: del(22)(qterq13.3)
    Breakpoints Information:
    Second Breakpoint:
    Location: q13.3
    Exact position: Chr22: 51122208bp
    This breakpoint occurs in intron 8 of NM_001080420.1.
    Junction Sequence is Unavailable
    Experimental Method: FISH, RT-PCR, CGH
    Reference Information
    PubMed ID: 16284256
    Authors: Bonaglia MC,Giorda R,Mani E,Aceti G,Anderlid BM,Baroncini A,Pramparo T,Zuffardi O
    Journal: Journal of medical genetics
    Go to Genome Browser ( Click the image )