DbCRID

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.

See also

Chromosome rearrangements

External links

http://dbCRID.biolead.org

v · d · eGenetics: chromosomes

General
Karyotype · Ploidy · Meiosis

Classification
Autosome · Sex chromosome · Microchromosome

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

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

v · d · ePathology: chromosome abnormalities (Q90–Q99 · 758)

Autosomal

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

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

Categories:
Database stubs
Biological databases
Chromosomes
Cytogenetics

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

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Chromosomal translocation — of the 4th and 20th chromosome. In genetics, a chromosome translocation is a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes. A gene fusion may be created when the translocation joins two otherwise… … Wikipedia

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