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For information, get in touch with: Dott.ssa Paola Visconti
Email: paola.visconti@hsanmartino.it
   P. Romano, A. Manniello et al. Nucl Acids Res 2009 37:D925-D932.
DOI: doi:10.1093/nar/gkn730; PMID: 18927105

Short description of cell lines
Tissue/organ: lymphoblast


- By clicking on the cell line name, you will retrieve the detailed description of the cell line
- By clicking on one of the terms between parentheses, you will retrieve the list of all relevant cell lines

26 CB1 (baboon, Papio hamadryas) - ECACC
81.3 (human) - ECACC
AC2 (mouse) - ECACC
CESS (human, leukemia, myelomonocytic) - ECACC
IGL001/01 (human, Caucasian) - GEIMM
IGL001/91 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGL001/92 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGL001/93 (human, Caucasian, fucosidosis) - GEIMM
IGL001/95 (human, Caucasian) - GEIMM
IGL001/96 (human, Caucasian, Wolman disease/cholesterol ester storage disease) - GEIMM
IGL001/97 (human, Caucasian) - GEIMM
IGL001/98 (human, Caucasian) - GEIMM
IGL001/99 (human, Caucasian) - GEIMM
IGL002/00 (human, Caucasian) - GEIMM
IGL002/01 (human, Caucasian) - GEIMM
IGL002/91 (human, Caucasian) - GEIMM
IGL002/92 (human, Caucasian, Aicardi syndrome / corpus callosum) - GEIMM
IGL002/93 (human, Caucasian, fucosidosis) - GEIMM
IGL002/94 (human, Caucasian) - GEIMM
IGL002/96 (human, Caucasian) - GEIMM
IGL002/98 (human, Caucasian) - GEIMM
IGL002/99 (human, Caucasian) - GEIMM
IGL003/00 (human, Caucasian) - GEIMM
IGL003/01 (human, Caucasian) - GEIMM
IGL003/91 (human, Caucasian) - GEIMM
IGL003/92 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGL003/93 (human, Caucasian) - GEIMM
IGL003/95 (human, Caucasian, glycogen storage disease II) - GEIMM
IGL003/96 (human, Caucasian, Berardinelli syndrome /seip syndrome) - GEIMM
IGL003/97 (human, Caucasian) - GEIMM
IGL003/98 (human, Caucasian) - GEIMM
IGL003/99 (human, Caucasian, methylenetetra-hydrofolate reductase def.) - GEIMM
IGL004/00 (human, Caucasian) - GEIMM
IGL004/01 (human, Caucasian) - GEIMM
IGL004/91 (human, Caucasian) - GEIMM
IGL004/93 (human, Caucasian) - GEIMM
IGL004/94 (human, Caucasian, autoimmune polyendocrinopathy syndrome,type I) - GEIMM
IGL004/96 (human, Caucasian) - GEIMM
IGL004/97 (human, Caucasian) - GEIMM
IGL004/98 (human, Caucasian) - GEIMM
IGL004/99 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL005/00 (human, Caucasian) - GEIMM
IGL005/01 (human, Caucasian) - GEIMM
IGL005/91 (human, Caucasian, mucopolysaccharidosis type III B) - GEIMM
IGL005/92 (human, Caucasian, articular hypermobility syndrome) - GEIMM
IGL005/93 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGL005/95 (human, Caucasian) - GEIMM
IGL005/97 (human, Caucasian) - GEIMM
IGL005/98 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGL005/99 (human, Caucasian) - GEIMM
IGL006/00 (human, Caucasian) - GEIMM
IGL006/01 (human, Caucasian) - GEIMM
IGL006/92 (human, Caucasian) - GEIMM
IGL006/93 (human, Caucasian) - GEIMM
IGL006/95 (human, Caucasian) - GEIMM
IGL006/97 (human, Caucasian) - GEIMM
IGL006/98 (human, Caucasian, glycogen storage disease II) - GEIMM
IGL006/99 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL007/00 (human, Caucasian) - GEIMM
IGL007/01 (human, Caucasian) - GEIMM
IGL007/91 (human, Caucasian, Krabbe disease) - GEIMM
IGL007/92 (human, Caucasian) - GEIMM
IGL007/94 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL007/96 (human, Caucasian) - GEIMM
IGL007/98 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL007/99 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL008/00 (human, Caucasian, salla disease) - GEIMM
IGL008/92 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGL008/93 (human, Caucasian, Alagille syndrome) - GEIMM
IGL008/94 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGL008/96 (human, Caucasian) - GEIMM
IGL008/98 (human, Caucasian) - GEIMM
IGL008/99 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL009/00 (human, Caucasian) - GEIMM
IGL009/01 (human, Caucasian) - GEIMM
IGL009/92 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGL009/96 (human, Caucasian, acyl-CoA dehydrogenase, long-chain, deficiency) - GEIMM
IGL009/97 (human, Caucasian) - GEIMM
IGL009/99 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL010/00 (human, Caucasian) - GEIMM
IGL010/92 (human, Caucasian) - GEIMM
IGL010/94 (human, Caucasian) - GEIMM
IGL010/98 (human, Caucasian) - GEIMM
IGL010/99 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGL011/00 (human, Caucasian) - GEIMM
IGL011/01 (human, Caucasian) - GEIMM
IGL011/96 (human, Caucasian) - GEIMM
IGL011/97 (human, Caucasian) - GEIMM
IGL011/98 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL011/99 (human, Caucasian, mucopolysaccharidosis type III A) - GEIMM
IGL012/00 (human, Caucasian) - GEIMM
IGL012/01 (human, Caucasian) - GEIMM
IGL012/95 (human, Caucasian, Wolman disease/cholesterol ester storage disease) - GEIMM
IGL012/97 (human, Caucasian) - GEIMM
IGL012/98 (human, Caucasian) - GEIMM
IGL012/99 (human, Caucasian) - GEIMM
IGL013/00 (human, Caucasian) - GEIMM
IGL013/01 (human, Caucasian) - GEIMM
IGL013/95 (human, Caucasian) - GEIMM
IGL013/96 (human, Caucasian) - GEIMM
IGL013/97 (human, Caucasian) - GEIMM
IGL013/98 (human, Caucasian, mucopolysaccharidosis type III C) - GEIMM
IGL013/99 (human, Caucasian) - GEIMM
IGL014/00 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL014/01 (human, Caucasian) - GEIMM
IGL014/95 (human, Caucasian) - GEIMM
IGL014/96 (human, Caucasian) - GEIMM
IGL014/97 (human, Caucasian) - GEIMM
IGL014/98 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGL014/99 (human, Caucasian, mucopolysaccharidosis type II) - GEIMM
IGL015/00 (human, Caucasian) - GEIMM
IGL015/01 (human, Caucasian) - GEIMM
IGL015/96 (human, Caucasian) - GEIMM
IGL015/97 (human, Caucasian) - GEIMM
IGL015/98 (human, Caucasian) - GEIMM
IGL015/99 (human, Caucasian) - GEIMM
IGL016/00 (human, Caucasian) - GEIMM
IGL016/01 (human, Caucasian) - GEIMM
IGL016/96 (human, Caucasian) - GEIMM
IGL016/97 (human, Caucasian) - GEIMM
IGL016/98 (human, Caucasian) - GEIMM
IGL016/99 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL017/00 (human, Caucasian) - GEIMM
IGL017/01 (human, Caucasian) - GEIMM
IGL017/96 (human, Caucasian, glycogen storage disease II) - GEIMM
IGL017/97 (human, Caucasian) - GEIMM
IGL017/98 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGL017/99 (human, Caucasian) - GEIMM
IGL018/96 (human, Caucasian) - GEIMM
IGL018/97 (human, Caucasian) - GEIMM
IGL018/98 (human, Caucasian, Gaucher disease type II) - GEIMM
IGL018/99 (human, Caucasian) - GEIMM
IGL019/00 (human, Caucasian) - GEIMM
IGL019/96 (human, Caucasian) - GEIMM
IGL019/97 (human, Caucasian) - GEIMM
IGL019/98 (human, Caucasian, Gaucher disease type II) - GEIMM
IGL019/99 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGL020/96 (human, Caucasian) - GEIMM
IGL020/98 (human, Caucasian, Wolman disease/cholesterol ester storage disease) - GEIMM
IGL020/99 (human, Caucasian) - GEIMM
IGL021/96 (human, Caucasian) - GEIMM
IGL021/98 (human, Caucasian) - GEIMM
IGL021/99 (human, Caucasian) - GEIMM
IGL022/00 (human, Caucasian) - GEIMM
IGL022/96 (human, Caucasian) - GEIMM
IGL022/98 (human, Caucasian) - GEIMM
IGL022/99 (human, Caucasian) - GEIMM
IGL023/00 (human, Caucasian) - GEIMM
IGL023/96 (human, Caucasian) - GEIMM
IGL023/98 (human, Caucasian) - GEIMM
IGL023/99 (human, Caucasian) - GEIMM
IGL024/00 (human, Caucasian) - GEIMM
IGL024/96 (human, Caucasian) - GEIMM
IGL024/98 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL024/99 (human, Caucasian) - GEIMM
IGL025/00 (human, Caucasian, SURF1) - GEIMM
IGL025/98 (human, Caucasian, mucopolysaccharidosis type IV A) - GEIMM
IGL025/99 (human, Caucasian) - GEIMM
IGL026/00 (human, Caucasian) - GEIMM
IGL026/99 (human, Caucasian) - GEIMM
IGL027/00 (human, Caucasian) - GEIMM
IGL027/98 (human, Caucasian, neuropathy, giant axonal) - GEIMM
IGL027/99 (human, Caucasian) - GEIMM
IGL028/00 (human, Caucasian) - GEIMM
IGL028/98 (human, Caucasian, Gaucher disease type III) - GEIMM
IGL028/99 (human, Caucasian) - GEIMM
IGL029/00 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL029/98 (human, Caucasian) - GEIMM
IGL029/99 (human, Caucasian) - GEIMM
IGL030/00 (human, Caucasian, Gaucher disease type II) - GEIMM
IGL030/98 (human, Caucasian) - GEIMM
IGL030/99 (human, Caucasian) - GEIMM
IGL031/00 (human, Caucasian) - GEIMM
IGL031/98 (human, Caucasian) - GEIMM
IGL031/99 (human, Caucasian, Gaucher disease type I) - GEIMM
IGL032/00 (human, Caucasian) - GEIMM
IGL032/98 (human, Caucasian) - GEIMM
IGL032/99 (human, Caucasian) - GEIMM
IGL033/00 (human, Caucasian) - GEIMM
IGL033/98 (human, Caucasian) - GEIMM
IGL033/99 (human, Caucasian) - GEIMM
IGL034/00 (human, Caucasian, Niemann-Pick disease, type C) - GEIMM
IGL034/99 (human, Caucasian) - GEIMM
IGL035/00 (human, Caucasian, spastic paraparesis) - GEIMM
IGL035/99 (human, Caucasian) - GEIMM
IGL036/99 (human, Caucasian) - GEIMM
IGL037/99 (human, Caucasian) - GEIMM
IGL038/99 (human, Caucasian) - GEIMM
IGL039/99 (human, Caucasian) - GEIMM
IGL040/99 (human, Caucasian) - GEIMM
IGL041/99 (human, Caucasian) - GEIMM
P3X63Ag8 (mouse, BALB/c, myeloma) - ICLC
RAMOS-AW (human, lymphoma, Burkitt) - ECACC
RAMOS-EHRB (human, lymphoma, Burkitt) - ECACC
RPMI 7666 (human, Caucasian) - ECACC
Subclone 707 BUF (mouse, leukemia, Friend) - ECACC
Subclone 707 DAP8 (mouse, leukemia, Friend) - ECACC
Subclone 707 DK 4.8 (mouse, leukemia, Friend) - ECACC
Subclone 707 DKA (mouse, leukemia, Friend) - ECACC
Subclone 707 DKE (mouse, leukemia, Friend) - ECACC
Subclone 707 DKH (mouse, leukemia, Friend) - ECACC
Subclone 707 DKJ (mouse, leukemia, Friend) - ECACC
Subclone 707 TG1 (mouse, leukemia, Friend) - ECACC
Subclone 707 TG2 (mouse, leukemia, Friend) - ECACC
TK6 (human) - ECACC
TK6TGR (human) - ECACC

For information, get in touch with:
IRCCS Ospedale Policlinico San Martino
Largo Rosanna Benzi, 10 - I-16132 Genova - Italy
Dott.ssa Paola Visconti
Email: paola.visconti@hsanmartino.it

If you want to cite CLDB and HyperCLDB, please use the following reference:

P. Romano, A. Manniello, O. Aresu, M. Armento, M. Cesaro, B. Parodi.
Cell Line Data Base: structure and recent improvements towards molecular authentication of human cell lines.
Nucleic Acids Research 2009 37(Database issue):D925-D932.
DOI: doi:10.1093/nar/gkn730; PMID: 18927105