DbCRID

dbCRID

Content
Description	chromosomal rearrangements in human diseases.
Organisms	Homo sapiens
Contact
Laboratory	Biolead.org Research Group, LC Science
Authors	Fanlou Kong
Primary citation	Kong & al. (2011)[1]
Release date	2010
Access
Website	http://dbCRID.biolead.org
Tools
Miscellaneous

The Chromosomal Rearrangements In Diseases (dbCRID) is a database of human chromosome rearrangements events and diseases related to them.^[1]

See also

• Chromosome rearrangements

References

1. ↑ 1.0 1.1 Kong, Fanlou; Zhu Jing, Wu Jun, Peng Jianjian, Wang Ying, Wang Qing, Fu Songbin, Yuan Li-Lian, Li Tongbin (Jan 2011). "dbCRID: a database of chromosomal rearrangements in human diseases". Nucleic Acids Res. (in eng) (England) 39 (Database issue): D895–900. doi:10.1093/nar/gkq1038. PMC 3013658. PMID 21051346.  Cite uses deprecated parameters (help)

External links

• http://dbCRID.biolead.org

v t e Genetics: chromosomes General Karyotype Ploidy Meiosis Classification Autosome Sex chromosome Microchromosome Circular chromosome Linear chromosome Polytene chromosome B chromosome Evolution Chromosomal inversion Chromosomal translocation Polyploidy Paleopolyploidy Structure Nucleosome Telomere: Telomere-binding protein (TINF2) Chromatid Chromatin Euchromatin Heterochromatin Histone H1 H2A H2B H3 H4 Centromere A B C1 C2 E F H I J K M N O P Q T See also List of organisms by chromosome count List of chromosome lengths for various organisms List of sequenced genomes B strc: edmb (perx), skel (ctrs), epit, cili, mito, nucl (chro)

v t e Pathology: chromosome abnormalities (Q90–Q99, 758) Autosomal Trisomies Down syndrome 21 Edwards syndrome 18 Patau syndrome 13 Trisomy 9 Warkany syndrome 2 8 Cat eye syndrome 22 Trisomy 16 Monosomies/deletions 1q21.1 deletion syndrome/1q21.1 duplication syndrome/TAR syndrome 1 Wolf-Hirschhorn syndrome 4 Cri du chat/Chromosome 5q deletion syndrome 5 Williams syndrome 7 Jacobsen syndrome 11 Miller–Dieker syndrome/Smith–Magenis syndrome 17 DiGeorge syndrome 22 22q11.2 distal deletion syndrome 22 22q13 deletion syndrome 22 genomic imprinting Angelman syndrome/Prader–Willi syndrome (15) Distal 18q-/Proximal 18q- X/Y linked Monosomy Turner syndrome (XO) Trisomy/tetrasomy, other karyotypes/mosaics Klinefelter syndrome (47,XXY) 48,XXYY 48,XXXY 49,XXXYY 49,XXXXY Triple X syndrome (47,XXX) 48,XXXX 49,XXXXX 47,XYY 48,XYYY 49,XYYYY 46,XX/XY Translocations Leukemia/lymphoma Lymphoid Burkitt's lymphoma t(8 MYC;14 IGH) Follicular lymphoma t(14 IGH;18 BCL2) Mantle cell lymphoma/Multiple myeloma t(11 CCND1:14 IGH) Anaplastic large cell lymphoma t(2 ALK;5 NPM1) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL; 22 BCR) Acute myeloblastic leukemia with maturation t(8 RUNX1T1;21 RUNX1) Acute promyelocytic leukemia t(15 PML,17 RARA) Acute megakaryoblastic leukemia t(1 RBM15;22 MKL1) Other Ewing's sarcoma t(11 FLI1; 22 EWS) Synovial sarcoma t(x SYT;18 SSX) Dermatofibrosarcoma protuberans t(17 COL1A1;22 PDGFB) Myxoid liposarcoma t(12 DDIT3; 16 FUS) Desmoplastic small round cell tumor t(11 WT1; 22 EWS) Alveolar rhabdomyosarcoma t(2 PAX3; 13 FOXO1) t (1 PAX7; 13 FOXO1) Other Fragile X syndrome Uniparental disomy XX male syndrome Ring chromosome (13; 14; 15; 20)