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: 10770 ( Case ID: 11601 )
    Disease: Hereditary Spastic Paraplegia ( DOID: 2476 )
    Event Information
    Precision: A
    Chromosome Rearrangement Type: Deletion
    Chromosome: 16
    Karyotype: del(16)(q24.3q24.3)
    Breakpoints Information:
    First Breakpoint:
    Location: q24.3
    Exact position: Chr16: 89612587bp
    This breakpoint occurs in intron10 of NM_003119.2.
    Second Breakpoint:
    Location: q24.3
    Exact position: Chr16: 89617759bp
    This breakpoint occurs in intron13 of NM_003119.2.
    Length of Deletion Segment is 5144bp.
    Junction Sequence is Unavailable
    Experimental Method: PCR, DNA sequencing
    Reference Information
    PubMed ID: 18200586
    Authors: Arnoldi A,Tonelli A,Crippa F,Villani G,Pacelli C,Sironi M,Pozzoli U,D'Angelo MG,Meola G,Martinuzzi A,Crimella C,Redaelli F,Panzeri C,Renieri A,Comi GP,Turconi AC,Bresolin N,Bassi MT
    Journal: Human mutation
    Go to Genome Browser ( Click the image )