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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

P 3 HR 1 (lymphoma, Burkitt) - IZSBS
P-190 (amnion, Edwards' syndrome / trisomy 18) - GGB
P-B88 (amnion, trisomy 21 / Down syndrome) - GGB
P-B91 (amnion, chromosome aberration) - GGB
P-B92 (amnion, chromosome aberration) - GGB
P-C96 (amnion, Edwards' syndrome / trisomy 18) - GGB
P-D89 (amnion) - GGB
P-D91 (amnion) - GGB
P-D94a (amnion, trisomy 21 / Down syndrome) - GGB
P-G96 (amnion, Edwards' syndrome / trisomy 18) - GGB
P-L92 (amnion, chromosome aberration) - GGB
P-NC94 (amnion) - GGB
P-R90 (amnion) - GGB
P-S90 (fibroblast, trisomy 21 / Down syndrome) - GGB
P-S96 (amnion) - GGB
P0894 (fibroblast, Edwards' syndrome / trisomy 18) - GGB
P1095 (chorionic villi, trisomy 21 / Down syndrome) - GGB
P1192 (fibroblast, Turner syndrome/noonan syndrome 1) - GGB
P12-ICHIKAWA (leukemia, T cell) - DSMZ
P1286 (fibroblast, trisomy 21 / Down syndrome) - GGB
P1294 (fibroblast) - GGB
P1392 (chorionic villi, chromosome aberration) - GGB
P1393 (chorionic villi, chromosome aberration) - GGB
P1985a (amnion, chondrodysplasia) - GGB
P1985f (amnion, chondrodysplasia) - GGB
P2092 (fibroblast) - GGB
P2189 (fibroblast) - GGB
P2190 (fibroblast) - GGB
P2594 (chorionic villi) - GGB
P3H3 (lymphoma, Burkitt) - MWIIW
P3HR-1 (lymph, lymphoma, Burkitt) - ECACC
P3HR-1 (lymphoma, Burkitt) - MWIIW
P92 (amnion, Prune Belly syndrome) - GGB
P93 (amnion, Turner syndrome/noonan syndrome 1) - GGB
P95 (amnion, Apert syndrome) - GGB
PA-1 (ovary, teratocarcinoma) - ECACC
PA-1 (ovary, teratocarcinoma) - GEICH
PA-1 (ovary, teratocarcinoma) - ICLC
PA-1 (ovary, teratocarcinoma) - SPBIC
PA-TU-8902 (pancreas, adenocarcinoma) - DSMZ
PA-TU-8988S (pancreas, adenocarcinoma) - DSMZ
PA-TU-8988T (pancreas, adenocarcinoma) - DSMZ
PA90P (lymphocyte) - GGB
PA94 (lymphocyte) - GGB
PA95P (lymphocyte) - GGB
PA96 (lymphocyte, hypercholesterolemia, familial) - GGB
PANC-1 (pancreas, carcinoma) - ECACC
PANC-1 (pancreas, carcinoma) - IZSBS
PANC-1 (pancreas, carcinoma) - SPBIC
PBR86M (lymphocyte) - GGB
PC-14 (lung, adenocarcinoma) - ECACC
PC-3 (prostate, adenocarcinoma, grade IV) - ECACC
PC-3 (prostate, adenocarcinoma, grade IV) - ICLC
PC1296 (fibroblast) - GGB
PCA90M (lymphocyte) - GGB
PCV87M (lymphocyte) - GGB
PE86P (lymphocyte) - GGB
PE96 (lymphocyte, exostoses) - GGB
PEER (peripheral blood, leukemia, T cell) - DSMZ
PF-382 (leukemia, T cell) - DSMZ
PF-382 (pleural effusion, leukemia, T cell) - ICLC
PF187 (fibroblast, trisomy 21 / Down syndrome) - GGB
PF90F (lymphocyte) - GGB
PF97387 (lymphocyte, B) - ICLC
PG91 (fibroblast, trisomy 21 / Down syndrome) - GGB
PGA86M (lymphocyte) - GGB
PI86 (lymphocyte, trisomy 21 / Down syndrome) - GGB
PL90 (lymphocyte) - GGB
PLB-985 (peripheral blood, leukemia, acute myeloid) - DSMZ
PLC/PRF/5 (liver, hepatoma) - ECACC
PLC/PRF/5 (liver, hepatoma, Alexander cells) - IZSBS
PLC/PRF/5 (Alexander cells) (liver, hepatoma) - MWIIW
PLC/PRF/5 (Alexander cells) (liver, hepatoma) - NAUBC
PM195 (lymphocyte) - GGB
PM85 (fibroblast) - GGB
PM87f (fibroblast) - GGB
PM87IL2 (lymphocyte) - GGB
PM89 (lymphocyte, trisomy 21 / Down syndrome) - GGB
PM91 (fibroblast, Turner syndrome, mosaic) - GGB
PM95 (lymphocyte) - GGB
PMA95M (lymphocyte) - GGB
PN86 (lymphocyte, chromosome aberration) - GGB
PNT1A (prostate) - ECACC
PNT2 (prostate) - ECACC
PR82 (fibroblast) - GGB
PR86S (lymphocyte) - GGB
PS192 (amnion, Prune Belly syndrome) - GGB
PS87P (lymphocyte) - GGB
PS92 (fibroblast, Fanconi anemia) - GGB
PS94 (lymphocyte) - GGB
PS95 (lymphocyte, Melnick-Needles syndrome) - GGB
PSN1 (pancreas, adenocarcinoma) - ECACC
PSN1 (pancreas, adenocarcinoma) - ICLC
PV95 (lymphocyte) - GGB
PVBC-CL247 (skin, fibroblast, cutis laxa) - PVUTC
PVBC-CL248 (skin, fibroblast, cutis laxa) - PVUTC
PVBC-EDS120 (skin, fibroblast, Ehlers-Danlos syndrome, type IV, autosomal dominant) - PVUTC
PVBC-EDS147 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS148 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS149 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS150 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS155 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS170 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS188 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS203 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS211 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS213 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS220 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS223 (skin, fibroblast, Ehlers-Danlos syndrome, type VI) - PVUTC
PVBC-EDS27 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS285 (skin, fibroblast, Ehlers-Danlos syndrome) - PVUTC
PVBC-EDS487 (skin, fibroblast, Ehlers-Danlos syndrome, type III) - PVUTC
PVBC-EDS528 (skin, fibroblast, Ehlers-Danlos syndrome, type IV, autosomal dominant) - PVUTC
PVBC-EDS546 (skin, fibroblast, Ehlers-Danlos syndrome, type IV, autosomal dominant) - PVUTC
PVBC-EDS547 (skin, fibroblast, Ehlers-Danlos syndrome, type IV, autosomal dominant) - PVUTC
PVBC-EDS550 (skin, fibroblast, Ehlers-Danlos syndrome, type III) - PVUTC
PVBC-I385 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-MF115 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF255 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF256 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF257 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF267 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF268 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF269 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF270 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF354 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF375 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF376 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF377 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF422 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF423 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF424 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF448 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-MF538 (skin, fibroblast, Marfan syndrome) - PVUTC
PVBC-OI (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI108 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI121 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI127 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI129 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI133 (skin, fibroblast, osteogenesis imperfecta, atypical) - PVUTC
PVBC-OI157 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI158 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI159 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI160 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI161 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI164 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI165 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI172 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI184 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI185 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI186 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI187 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI189 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI193 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI197 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI204 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI205 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI206 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI217 (skin, fibroblast, osteogenesis imperfecta) - PVUTC
PVBC-OI227 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI228 (skin, fibroblast, osteogenesis imperfecta) - PVUTC
PVBC-OI230 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI234 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI250 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI254 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI265 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI271 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI272 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI273 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI274 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI275 (skin, fibroblast, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI276 (skin, fibroblast, osteogenesis imperfecta, type I/EDS, atypical) - PVUTC
PVBC-OI277 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI284 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI291 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI299 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI305 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI306 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI307 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI313 (skin, fibroblast, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI314 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI317 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI325 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI330 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI332 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI340 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI347 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI348 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI350 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI356 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI370 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI371 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI373 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI378 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI379 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI380 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI383 (skin, fibroblast, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI384 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI387 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI388 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI396 (skin, fibroblast) - PVUTC
PVBC-OI427 (skin, fibroblast) - PVUTC
PVBC-OI428 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI433 (skin, fibroblast) - PVUTC
PVBC-OI437 (skin, fibroblast) - PVUTC
PVBC-OI440 (skin, fibroblast, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI443 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI444 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI449 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI452 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI453 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI460 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI461 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI462 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI464 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI465 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI466 (skin, fibroblast, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI467 (skin, fibroblast, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI471 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI488 (skin, fibroblast) - PVUTC
PVBC-OI489 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI499 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI500 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI522 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-OI531 (skin, fibroblast, osteogenesis imperfecta, type I/EDS, atypical) - PVUTC
PVBC-OI535 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI540 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI55 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI553 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI555 (skin, fibroblast, osteogenesis imperfecta, type I (with blue sclerae)) - PVUTC
PVBC-OI559 (skin, fibroblast, osteogenesis imperfecta, type II) - PVUTC
PVBC-OI65 (skin, fibroblast, osteogenesis imperfecta, type IV) - PVUTC
PVBC-OI82 (skin, fibroblast, osteogenesis imperfecta, type III with normal sclerae) - PVUTC
PVBC-Pr110 (skin, fibroblast, prolidase deficiency) - PVUTC
PVBC-Pr152 (skin, fibroblast, prolidase deficiency) - PVUTC
PVBC-Pr260 (skin, fibroblast, prolidase deficiency) - PVUTC
PVBC-Pr98 (skin, fibroblast, prolidase deficiency) - PVUTC
PVCB-EDS516 (skin, fibroblast, Ehlers-Danlos syndrome, type IV, autosomal dominant) - PVUTC
PX92 (pseudoxanthoma elasticum) - 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