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For information, get in touch with: Dott.ssa Barbara Parodi
Email: barbara.parodi@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: lymphocyte


- 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

A84M (human, Caucasian) - GGB
A84P (human, Caucasian) - GGB
A94M (human, Caucasian) - GGB
A94P (human, Caucasian) - GGB
AAA95M (human, Caucasian) - GGB
AC84 (human, Caucasian, thanatophoric dwarfism) - GGB
AC95 (human, Caucasian, cri du chat syndrome) - GGB
AD94IL2 (human, Caucasian) - GGB
AD94LEBV (human, Caucasian) - GGB
AFA95M (human, Caucasian) - GGB
AG95P (human, Caucasian) - GGB
AJ95 (human, Caucasian, corpus callosum agenesis) - GGB
ALM86M (human, Caucasian) - GGB
AM85 (human, Caucasian) - GGB
AM86 (human, Caucasian) - GGB
AM95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
AN86P (human, Caucasian) - GGB
AP95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
AR84S (human, Caucasian) - GGB
AT95 (human, Caucasian, malformations) - GGB
B86M (human, Caucasian) - GGB
BA 93 (human, Caucasian) - GGB
BA193 (human, Caucasian) - GGB
BA96 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
BB96P (human, Caucasian) - GGB
BC87IL2 (human, Caucasian) - GGB
BC87ls (human, Caucasian) - GGB
BF93 (human, Caucasian) - GGB
BF95 (human, Caucasian) - GGB
BF96 (human, Caucasian) - GGB
BG194 (human, Caucasian) - GGB
BGF96M (human, Caucasian) - GGB
BGP94 (human, Caucasian) - GGB
BI96 (human, Caucasian, tuberous sclerosis) - GGB
BL95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
BLE96 (human, Caucasian, tuberous sclerosis) - GGB
BLN96M (human, Caucasian) - GGB
BM87 (human, Caucasian) - GGB
BM95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
BP86 (human, Caucasian, chromosome aberration) - GGB
BP96 (human, Caucasian, tuberous sclerosis) - GGB
BR96P (human, Caucasian) - GGB
C0994IL2 (human, Caucasian, chromosome aberration) - GGB
C5MJ (human) - RMUFM
C86M (human, Caucasian) - GGB
C86P (human, Caucasian) - GGB
C91PL (human) - RMUFM
CA295 (human, Caucasian) - GGB
CA95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
CA96 (human, Caucasian, familial epylepsy) - GGB
CC96 (human, Caucasian, neurofibromatosis type I) - GGB
CCM89M (human, Caucasian) - GGB
CD86 (human) - GGB
CD88ls (human, Caucasian, Down syndrome, mosaic) - GGB
CDM96 (human, Caucasian, familial epylepsy) - GGB
CF84ls (human, Caucasian, Down syndrome, mosaic) - GGB
CF89P (human, Caucasian) - GGB
CF96F (human, Caucasian) - GGB
CF96P (human, Caucasian) - GGB
CG89 (human, Caucasian, chromosome aberration) - GGB
CG94IL2 (human, Caucasian, chromosome aberration) - GGB
CG96 (human, Caucasian, neurofibromatosis type I) - GGB
CL95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
CL96IL2 (human, Caucasian, familial epylepsy) - GGB
CLM96M (human, Caucasian) - GGB
CM86 (human, trisomy 21 / Down syndrome) - GGB
CM87 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
CM87IL2 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
CM88M (human, Caucasian) - GGB
CM91IL2 (human, Caucasian, chromosome aberration) - GGB
CM91ls (human, Caucasian, Turner syndrome/noonan syndrome 1) - GGB
CM94 (human, Caucasian) - GGB
CM94P (human, Caucasian) - GGB
CMR94M (human, Caucasian) - GGB
CN96 (human, Caucasian) - GGB
CR86 (human, trisomy 21 / Down syndrome) - GGB
CR88P (human, Caucasian) - GGB
CR96 (human, Caucasian, epilepsy) - GGB
CT96 (human, Caucasian, hypercholesterolemia, familial) - GGB
CV96F (human, Caucasian) - GGB
CVD89M (human, Caucasian) - GGB
DBC95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
DBM96 (human, Caucasian, neurofibromatosis type I) - GGB
DBV95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
DC96 (human, Caucasian, familial epylepsy) - GGB
DCi96 (human, Caucasian, familial epylepsy) - GGB
DCo96 (human, Caucasian, familial epylepsy) - GGB
DCon96 (human, Caucasian, familial epylepsy) - GGB
DE96P (human, Caucasian) - GGB
DFA96M (human, Caucasian) - GGB
DFC96 (human, Caucasian, familial epylepsy) - GGB
DFF87 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
DFGe96 (human, Caucasian, familial epylepsy) - GGB
DFGi96 (human, Caucasian, familial epylepsy) - GGB
DG96 (human, Caucasian, familial epylepsy) - GGB
DLG96IL2 (human, Caucasian, Down syndrome, mosaic) - GGB
DM94 (human, Caucasian, Angelman syndrome) - GGB
DMM87 (human, Caucasian) - GGB
DR89P (human, Caucasian) - GGB
DVA96 (human, Caucasian, familial epylepsy) - GGB
FC96IL2 (human, Caucasian) - GGB
FC96ls (human, Caucasian) - GGB
FE92 (human, Caucasian) - GGB
FFC87M (human, Caucasian) - GGB
FG86 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
FGC95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
FGF96 (human, Caucasian, neurofibromatosis type I) - GGB
FL88 (human, Caucasian) - GGB
FMG87 (human, Caucasian) - GGB
FN86 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
G25496 (human, Caucasian, hypercholesterolemia, familial) - GGB
GA93 (human, Caucasian) - GGB
GA96 (human, Caucasian, neurofibromatosis type I) - GGB
GAa85F (human, Caucasian) - GGB
GAi85F (human, Caucasian) - GGB
GB95 (human, Caucasian, hypercholesterolemia, familial) - GGB
GC95 (human, Caucasian, hypercholesterolemia, familial) - GGB
GE86 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
GE95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
GG87 (human, Caucasian) - GGB
GGP87F (human, Caucasian) - GGB
GI95 (human, Caucasian, hypercholesterolemia, familial) - GGB
GM87 (human, Caucasian) - GGB
GM95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
GR95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
GS83ls (human, Caucasian, Down syndrome, mosaic) - GGB
GT186ls (human, Caucasian, hermaphroditism true) - GGB
GT86ls (human, Caucasian) - GGB
IC86 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
IG88IL2 (human, Caucasian) - GGB
IG88ls (human, Caucasian) - GGB
IS94 (human, Caucasian) - GGB
IV95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
L89M (human, Caucasian) - GGB
L89P (human, Caucasian) - GGB
L90 (human, Caucasian, Huntington chorea) - GGB
LA96 (human, Caucasian, tuberous sclerosis) - GGB
LAn96 (human, Caucasian, tuberous sclerosis) - GGB
Lb 224 (human, Caucasian) - NAUBC
Lb 23 (human, Caucasian, mucopolysaccharidosis type II) - NAUBC
Lb 24 (human, Caucasian, mucopolysaccharidosis type II) - NAUBC
Lb 752 (human, Caucasian, mucopolysaccharidosis type III B) - NAUBC
LBE88 (human, Caucasian) - GGB
LM96 (human, Caucasian, tuberous sclerosis) - GGB
LMas96 (human, Caucasian, tuberous sclerosis) - GGB
LP96 (human, Caucasian, tuberous sclerosis) - GGB
LT89 (human, Caucasian, Martin-Bell syndrome) - GGB
LT94 (human, Caucasian, Fanconi anemia) - GGB
M-G89 (human, Caucasian, chromosome aberration) - GGB
MA86 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
MA94IL2 (human, Caucasian, Fanconi anemia) - GGB
MA94LEBV (human, Caucasian, Fanconi anemia) - GGB
MAM94M (human, Caucasian) - GGB
MC86 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
MC94 (human, Caucasian) - GGB
MC96 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
MCR96M (human, Caucasian) - GGB
MCS94MIL2 (human, Caucasian) - GGB
MCS94MLEBV (human, Caucasian) - GGB
MCT95M (human, Caucasian) - GGB
MD86 (human, trisomy 21 / Down syndrome) - GGB
MD94PLEBV (human, Caucasian) - GGB
MD94SIL2 (human, Caucasian) - GGB
MD94SLEBV (human, Caucasian) - GGB
MD95 (human, Caucasian, Martin-Bell syndrome) - GGB
MDTC RP 19 (turkey, Marek's disease) - IZSBS
ME96 (human, Caucasian) - GGB
ME96P (human, Caucasian) - GGB
MG96No (human, Caucasian) - GGB
MGF89P (human, Caucasian) - GGB
MGL95 (human, Caucasian, Wolff mental retardation syndrome) - GGB
MGP96Na (human, Caucasian) - GGB
ML87P (human, Caucasian) - GGB
ML89S (human, Caucasian) - GGB
MLA87M (human, Caucasian) - GGB
MM87IL2 (human, Caucasian) - GGB
MM87ls (human, Caucasian) - GGB
MM96 (human, Caucasian, Martin-Bell syndrome) - GGB
MN95 (human, Caucasian, Martin-Bell syndrome) - GGB
MN96 (human, Caucasian) - GGB
MOM89M (human, Caucasian) - GGB
MP 1 (human, Caucasian) - ECBR
MP 10 (human, Caucasian) - ECBR
MP 12 (human, Caucasian) - ECBR
MP 14 (human, Caucasian) - ECBR
MP 3 (human, Caucasian) - ECBR
MP 4 (human, Caucasian) - ECBR
MP 5 (human, Caucasian) - ECBR
MP 6 (human, Caucasian) - ECBR
MP 8 (human, Caucasian) - ECBR
MP 9 (human, Caucasian) - ECBR
MP90 (human, Caucasian) - GGB
MP95P (human, Caucasian) - GGB
MPL96M (human, Caucasian) - GGB
MR87 (human, Caucasian) - GGB
MS95 (human, Caucasian) - GGB
MT-2 (human) - ECACC
MT2 (human) - RMUFM
MT89 (human, Caucasian) - GGB
NA95P (human, Caucasian) - GGB
NC95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
NF96 (human, Caucasian, hypercholesterolemia, familial) - GGB
NF96IL2 (human, Caucasian, hypercholesterolemia, familial) - GGB
NG96 (human, Caucasian, hypercholesterolemia, familial) - GGB
NG96IL2 (human, Caucasian, hypercholesterolemia, familial) - GGB
NH17 (human, leukemia, acute lymphoblastic T cell) - ECACC
NM94 (human, Caucasian, chromosome aberration) - GGB
NM95 (human, Caucasian) - GGB
NV96 (human, Caucasian, hypercholesterolemia, familial) - GGB
NV96IL2 (human, Caucasian, hypercholesterolemia, familial) - GGB
O88M (human, Caucasian) - GGB
O88P (human, Caucasian) - GGB
OL95 (human, Caucasian, Steinert disease) - GGB
OM87 (human, Caucasian, dimorphism) - GGB
OM87P (human, Caucasian) - GGB
OT87M (human, Caucasian) - GGB
PA90P (human, Caucasian) - GGB
PA94 (human, Caucasian) - GGB
PA95P (human, Caucasian) - GGB
PA96 (human, Caucasian, hypercholesterolemia, familial) - GGB
PBR86M (human, Caucasian) - GGB
PCA90M (human, Caucasian) - GGB
PCV87M (human, Caucasian) - GGB
PE86P (human, Caucasian) - GGB
PE96 (human, Caucasian, exostoses) - GGB
PF90F (human, Caucasian) - GGB
PGA86M (human, Caucasian) - GGB
PI86 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
PL90 (human, Caucasian) - GGB
PM195 (human, Caucasian) - GGB
PM87IL2 (human, Caucasian) - GGB
PM89 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
PM95 (human, Caucasian) - GGB
PMA95M (human, Caucasian) - GGB
PN86 (human, Caucasian, chromosome aberration) - GGB
PR86S (human, Caucasian) - GGB
PS87P (human, Caucasian) - GGB
PS94 (human, Caucasian) - GGB
PS95 (human, Caucasian, Melnick-Needles syndrome) - GGB
PUTKO (human / human, leukemia, myeloid) - ECACC
PV95 (human, Caucasian) - GGB
R-G96 (human, Caucasian) - GGB
RFE88 (human, Caucasian) - GGB
RM86 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
RMR96 (human, Caucasian) - GGB
SA87ls (human, Caucasian, Down syndrome, mosaic) - GGB
SA88ls (human, Caucasian, Fanconi anemia) - GGB
SBV86M (human, Caucasian) - GGB
SE95IL2 (human, Caucasian) - GGB
SE95ls (human, Caucasian) - GGB
SG88P (human, Caucasian) - GGB
SG94 (human, Caucasian) - GGB
SLC87M (human, Caucasian) - GGB
SM86P (human, Caucasian) - GGB
SMC87 (human, Caucasian) - GGB
SMC95S (human, Caucasian) - GGB
SP87M (human, Caucasian) - GGB
SR95F (human, Caucasian) - GGB
SS86 (human, Caucasian, severe combined immunodeficiency disease) - GGB
SS95 (human, Caucasian, tuberous sclerosis) - GGB
STA88M (human, Caucasian) - GGB
TC86P (human, Caucasian) - GGB
TC96 (human, Caucasian, chromosome aberration) - GGB
TLA96M (human, Caucasian) - GGB
TM 902 (mouse) - ECBR
TM 903 (mouse) - ECBR
TM94 (human, Caucasian, chromosome aberration) - GGB
TM95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
TM96P (human, Caucasian) - GGB
TR88 (human, Caucasian) - GGB
TR96 (human, Caucasian, hypercholesterolemia, familial) - GGB
TSF86M (human, Caucasian) - GGB
V-C89IL2 (human, Caucasian) - GGB
V-C89ls (human, Caucasian) - GGB
VA88 (human, Caucasian) - GGB
VA94 (human, Caucasian) - GGB
VB86P (human, Caucasian) - GGB
VBA88MIL2 (human, Caucasian) - GGB
VBA88Mls (human, Caucasian) - GGB
VG86 (human, Caucasian, chromosome aberration) - GGB
VL96 (human, Caucasian, neurofibromatosis type I) - GGB
VM89 (human, Caucasian) - GGB
VP94P (human, Caucasian) - GGB
VVM94M (human, Caucasian) - GGB
VVP86M (human, Caucasian) - GGB
ZDF95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB


For information, get in touch with:
IRCCS Ospedale Policlinico San Martino
Largo Rosanna Benzi, 10 - I-16132 Genova - Italy
Dott.ssa Barbara Parodi
Email: barbara.parodi@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