DbCRID

dbCRID

Content
Description	chromosomal rearrangements in human diseases.
Organism(s)	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]

References

^ ^a ^b 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" (in eng). Nucleic Acids Res. (England) 39 (Database issue): D895-900. doi:10.1093/nar/gkq1038. PMC 3013658. PMID 21051346. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3013658.

General

Classification

Evolution

Structure

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

B strc: edmb (perx), skel (ctrs), epit, cili, mito, nucl (chro)

Trisomies	Down syndrome (21) · Edwards syndrome (18) · Patau syndrome (13) Trisomy 9 · Trisomy 8/Warkany syndrome 2 (8) · Trisomy 22/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) · 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's 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

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

Other