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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
Species: human (all ethnic groups)


- 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 line

1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

G-292 Clone A141B1 (bone, osteosarcoma) - ECACC
G-361 (skin, malignant melanoma) - BGEBS
G-361 (skin, malignant melanoma) - ECACC
G-361 (skin, melanoma) - ICLC
G-401 (kidney) - ECACC
G-402 (kidney, leiomyoblastoma) - ECACC
G-A88 (amnion, trisomy 21 / Down syndrome) - GGB
G-B90 (amnion) - GGB
G-C195 (amnion, Edwards' syndrome / trisomy 18) - GGB
G-C92 (amnion, trisomy 21 / Down syndrome) - GGB
G-C94 (fibroblast, trisomy 21 / Down syndrome) - GGB
G-C95 (amnion, anencephaly) - GGB
G-F92a (amnion, trisomy 21 / Down syndrome) - GGB
G-F92f (fibroblast, trisomy 21 / Down syndrome) - GGB
G-F95 (amnion) - GGB
G-L88 (fibroblast, trisomy 21 / Down syndrome) - GGB
G-M89 (amnion, Edwards' syndrome / trisomy 18) - GGB
G-M95a (amnion, trisomy 21 / Down syndrome) - GGB
G-M95f (fibroblast, trisomy 21 / Down syndrome) - GGB
G0086 (fibroblast, trisomy 16) - GGB
G0895 (fibroblast, Patau syndrome / trisomy 13) - GGB
G1094 (fibroblast) - GGB
G1291 (fibroblast, trisomy 7) - GGB
G25496 (lymphocyte, hypercholesterolemia, familial) - GGB
GA87 (skin, fibroblast, trisomy 21 / Down syndrome) - GGB
GA93 (lymphocyte) - GGB
GA96 (lymphocyte, neurofibromatosis type I) - GGB
GAa85F (lymphocyte) - GGB
GAi85F (lymphocyte) - GGB
GAMG (glioma) - DSMZ
GB95 (lymphocyte, hypercholesterolemia, familial) - GGB
GBM (nervous system, glioblastoma) - MIISB
GC95 (lymphocyte, hypercholesterolemia, familial) - GGB
GCT (lung, metastasis, histiocytoma) - IZSBS
GDM-1 (peripheral blood, leukemia, acute myelomonocytic) - DSMZ
GDM-1 (peripheral blood, leukemia, acute myelomonocytic) - ICLC
GE86 (lymphocyte, trisomy 21 / Down syndrome) - GGB
GE95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
GF-D8 (peripheral blood, leukemia, acute myeloid) - ICLC
GG87 (lymphocyte) - GGB
GGP87F (lymphocyte) - GGB
GI-CA-N (neuroblastoma) - GEIOP
GI-LI-N (neuroblastoma) - GEIOP
GI-ME-N (neuroblastoma) - GEIOP
GI-ME-N (bone marrow, metastatic neuroblastoma, stage IV) - ICLC
GI95 (lymphocyte, hypercholesterolemia, familial) - GGB
GIRARDI HEART (heart) - ECACC
Girardi heart (heart) - IZSBS
GIRARDI HEART (heart) - SPBIC
GIRARDI HEART C2 (cervix, carcinoma) - DSMZ
GIRARDI HEART C7 (cervix, carcinoma) - DSMZ
GL-6 (251-MG) (glioblastoma) - MWIIW
GM 490 (lymphoma) - PSHIM
GM00112A (fibroblast, Niemann-Pick disease, type A) - MIECC
GM00135A (fibroblast, hypercholesterolemia, familial) - MIECC
GM00425 (skin, fibroblast) - BGEBS
GM00469 (fibroblast, adenosine deaminase) - MIECC
GM00483 (fibroblast, hypercholesterolemia, familial) - MIECC
GM00488C (fibroblast, hypercholesterolemia, familial) - MIECC
GM00637B (skin, fibroblast) - NAUBC
GM00638 (fibroblast, galactosemia) - MWIIW
GM00639 (fibroblast, galactosemia) - MWIIW
GM00863 (fibroblast, Wolman disease/cholesterol ester storage disease) - MIECC
GM00881 (fibroblast, angiokeratoma, diffuse / Fabry disease) - MIECC
GM01229 (skin, fibroblast) - BGEBS
GM01606A (fibroblast, Wolman disease/cholesterol ester storage disease) - MIECC
GM01607 (fibroblast, Gaucher disease type I) - MIECC
GM02185 (skin, fibroblast) - GEIMG
GM02290 (skin, fibroblast, Lesch-Nyhan syndrome) - MIISA
GM02291 (lung, embryonic, Lesch-Nyhan syndrome) - MIISA
GM02408C (fibroblast, hypercholesterolemia, familial) - MIECC
GM02605 (fibroblast) - GEIMG
GM02824 (fibroblast) - GEIMG
GM02848 (skin, fibroblast) - BGEBS
GM03123 (fibroblast, Niemann-Pick disease) - MIECC
GM03252 (fibroblast, Niemann-Pick disease, type B) - MIECC
GM05752 (fibroblast, Farber lipogranulomatosis) - MIECC
GM05870 (fibroblast, acyl-CoA dehydrogenase, medium-chain, deficiency) - MIECC
GM06127 (fibroblast, acyl-CoA dehydrogenase, long-chain, deficiency) - MIECC
GM08866 (fibroblast, acyl-CoA dehydrogenase, short-chain, deficiency) - MIECC
GM87 (lymphocyte) - GGB
GM95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
GP-16 (skin, fibroblast, pyroglutamicaciduria / 5-oxoprolinuria) - RMSTC
GP2d (colon, adenocarcinoma) - ECACC
GP5d (colon, adenocarcinoma) - ECACC
GR-M (skin, melanoma) - ECACC
GR95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
GS-109-V-20 (skin, fibroblast, Gardner's syndrome) - ECACC
GS-109-V-34 (skin, fibroblast, Gardner's syndrome) - ECACC
GS-109-V-63 (skin, fibroblast, Gardner's syndrome) - ECACC
GS83f (fibroblast, Down syndrome, mosaic) - GGB
GS83ls (lymphocyte, Down syndrome, mosaic) - GGB
GS93 (fibroblast, Fanconi anemia) - GGB
GT186f (fibroblast, hermaphroditism true) - GGB
GT186ls (lymphocyte, hermaphroditism true) - GGB
GT86f (fibroblast, hermaphroditism true) - GGB
GT86ls (lymphocyte) - GGB

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