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For information, get in touch with: Dott.ssa Assunta Manniello
Email: mariaassunta.manniello@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: fibroblast


- 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

14.012.8.1 (hamster, Syrian) - MWIIW
208F (rat, Fisher) - ECACC
3T3 (mouse, Swiss albino) - DSMZ
3T6 (mouse, Swiss albino) - DSMZ
598_81H (human, Caucasian) - GGB
A-A94 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
A-B92f (human, Caucasian) - GGB
A09194 (human, Caucasian, chromosome aberration) - GGB
A1594 (human, Caucasian, chromosome aberration) - GGB
A94 (human, Caucasian, camptomelic dwarfism) - GGB
A95 (human, Caucasian, dwarfism thanatophoric) - GGB
AA84F (human, Caucasian) - GGB
AE84S (human, Caucasian) - GGB
AR91 (human, Caucasian, Fanconi anemia) - GGB
B-B88f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B-M 92f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B-M91f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B-R93f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B192 (human, Caucasian, dyskeratosis) - GGB
B2195 (human, Caucasian, gastroschisis) - GGB
B84 (human, Caucasian) - GGB
B85 (human, Caucasian) - GGB
BC96 (human, Caucasian) - GGB
C-B95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
C-C87f (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
C-F89 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
C-M87 (human, Caucasian) - GGB
C-M92 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
C-N95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
C1191f (human, Caucasian, trisomy 14) - GGB
C1191v (human, Caucasian, trisomy 14) - GGB
C1192 (human, Caucasian, trisomy 7) - GGB
C1195 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
C1293 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
C1294f (human, Caucasian) - GGB
C1595f (human, Caucasian) - GGB
C83 (human, Caucasian) - GGB
C87 (human, Caucasian) - GGB
C91 (human, Caucasian, chromosome mosaic) - GGB
C92 (human, Caucasian, D. Becker syndrome) - GGB
C93 (human, Caucasian, Pallister Killian syndrome) - GGB
CD88f (human, Caucasian, Down syndrome, mosaic) - GGB
CD89P (human, Caucasian) - GGB
CF84f (human, Caucasian, Down syndrome, mosaic) - GGB
CL96f (human, Caucasian, erythroblastopenia, transient) - GGB
CR83 (human, Caucasian, epidermolysis bullo'sa) - GGB
CS191 (human, Caucasian, Turner syndrome, mosaic) - GGB
CS96 (human, Caucasian, Freeman-Sheldon syndrome) - GGB
D-A92f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
D-F92 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
D-G92 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
D0994 (human, Caucasian) - GGB
D1589 (human, Caucasian) - GGB
D2085 (human, Caucasian) - GGB
D2187 (human, Caucasian, anencephaly) - GGB
D94 (human, Caucasian, Miller-Dieker syndrome) - GGB
D96 (human, Caucasian) - GGB
DA94 (human, Caucasian, Patau syndrome / trisomy 13) - GGB
DL86 (human, Caucasian, severe combined immunodeficiency disease) - GGB
DL87 (human, Caucasian) - GGB
DLF87 (human, Caucasian) - GGB
DLG96f (human, Caucasian, Down syndrome, mosaic) - GGB
DLL87S (human, Caucasian) - GGB
DPS84 (human, Caucasian, osteogenesis imperfecta) - GGB
DS 92 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
EH/A44 (hamster, Syrian) - MWIIW
EHT (hamster, Syrian) - MWIIW
F-P95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
F0091 (human, Caucasian, trisomy 5) - GGB
F0894 (human, Caucasian) - GGB
F1187 (human, Caucasian, trisomy 16) - GGB
F1293 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
F1792 (human, Caucasian, hydrocephalus) - GGB
F2586 (human, Caucasian) - GGB
F89 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
F94 (human, Caucasian, camptomelic dwarfism) - GGB
F95 (human, Caucasian, Martin-Bell syndrome) - GGB
F96 (human, Caucasian, Marfan syndrome) - GGB
FG186 (human, Caucasian) - GGB
Flow 6000 (human) - PNIOS
FV93 (human, Caucasian, Turner syndrome/noonan syndrome 1) - GGB
G-C94 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
G-F92f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
G-L88 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
G-M95f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
G0086 (human, Caucasian, trisomy 16) - GGB
G0895 (human, Caucasian, Patau syndrome / trisomy 13) - GGB
G1094 (human, Caucasian) - GGB
G1291 (human, Caucasian, trisomy 7) - GGB
GM00112A (human, Caucasian, Niemann-Pick disease, type A) - MIECC
GM00135A (human, Caucasian, hypercholesterolemia, familial) - MIECC
GM00469 (human, Caucasian, adenosine deaminase) - MIECC
GM00483 (human, Caucasian, hypercholesterolemia, familial) - MIECC
GM00488C (human, Caucasian, hypercholesterolemia, familial) - MIECC
GM00638 (human, galactosemia) - MWIIW
GM00639 (human, Black, galactosemia) - MWIIW
GM00863 (human, Caucasian, Wolman disease/cholesterol ester storage disease) - MIECC
GM00881 (human, Caucasian, angiokeratoma, diffuse / Fabry disease) - MIECC
GM01606A (human, Wolman disease/cholesterol ester storage disease) - MIECC
GM01607 (human, Caucasian, Gaucher disease type I) - MIECC
GM02408C (human, hypercholesterolemia, familial) - MIECC
GM02605 (human, Caucasian) - GEIMG
GM02824 (human, Caucasian) - GEIMG
GM03123 (human, Caucasian, Niemann-Pick disease) - MIECC
GM03252 (human, Caucasian, Niemann-Pick disease, type B) - MIECC
GM05752 (human, Caucasian, Farber lipogranulomatosis) - MIECC
GM05870 (human, Caucasian, acyl-CoA dehydrogenase, medium-chain, deficiency) - MIECC
GM06127 (human, Caucasian, acyl-CoA dehydrogenase, long-chain, deficiency) - MIECC
GM08866 (human, Caucasian, acyl-CoA dehydrogenase, short-chain, deficiency) - MIECC
GS83f (human, Caucasian, Down syndrome, mosaic) - GGB
GS93 (human, Caucasian, Fanconi anemia) - GGB
GT186f (human, Caucasian, hermaphroditism true) - GGB
GT86f (human, Caucasian, hermaphroditism true) - GGB
I1094 (human, Caucasian) - GGB
I1686 (human, Caucasian) - GGB
I2586 (human, Caucasian, achondrogenesis I) - GGB
K22 (rat) - SPBIC
K29 (rat) - SPBIC
L (mouse) - GEICH
L-DR92f (human, Caucasian, chromosome aberration) - GGB
L-Z93f (human, Caucasian) - GGB
L1192 (human, Caucasian, Patau syndrome / trisomy 13) - GGB
L1296 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
L94 (human, Caucasian, Dyskeratosis congenita) - GGB
M-B87f (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
M-B95f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-L94 (human, Caucasian) - GGB
M-L95f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-M196 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-P91f (human, Caucasian, Fanconi anemia) - GGB
M-R89 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-T95f (human, Caucasian) - GGB
M-V94 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M1392 (human, Caucasian, chromosome aberration) - GGB
M1594 (human, Caucasian) - GGB
M83 (human, Caucasian) - GGB
M85 (human, Caucasian, hermaphroditism true) - GGB
M86 (human, Caucasian, anencephaly) - GGB
M90 (human, Caucasian) - GGB
MA91 (human, Caucasian, Fanconi anemia) - GGB
MC88 (human, Caucasian) - GGB
MF92 (human, Caucasian, osteogenesis imperfecta) - GGB
ML86 (human, Caucasian) - GGB
MM87f (human, Caucasian) - GGB
MRSV (AP170) (mouse) - NAUBP
N92 (human, Caucasian, dwarfism thanatophoric) - GGB
P-S90 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
P0894 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
P1192 (human, Caucasian, Turner syndrome/noonan syndrome 1) - GGB
P1286 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
P1294 (human, Caucasian) - GGB
P2092 (human, Caucasian) - GGB
P2189 (human, Caucasian) - GGB
P2190 (human, Caucasian) - GGB
PA317 (mouse, NIH Swiss) - ECACC
PA317 (mouse, NIH Swiss) - SPBIC
PC1296 (human, Caucasian) - GGB
PF187 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
PG91 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
PM85 (human, Caucasian) - GGB
PM87f (human, Caucasian) - GGB
PM91 (human, Caucasian, Turner syndrome, mosaic) - GGB
PR82 (human, Caucasian) - GGB
PS92 (human, Caucasian, Fanconi anemia) - GGB
Q-P96 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
Q1785 (human, Caucasian) - GGB
R-A95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
R-C95 (human, Caucasian, Patau syndrome / trisomy 13) - GGB
R-DC90f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
R-G94f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
R-P 91f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
R-S95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
R1391 (human, Caucasian) - GGB
R1487 (human, Caucasian, anencephaly) - GGB
R86 (human, Caucasian, Fanconi anemia) - GGB
RD91 (human, Caucasian, Down syndrome, mosaic) - GGB
RM91 (human, Caucasian, Pallister Killian syndrome) - GGB
RP88 (human, Caucasian, collagen disease) - GGB
S-D92f (human, Caucasian, Turner syndrome/noonan syndrome 1) - GGB
S-F95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
S-G94 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
S-L90f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
S-L95f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
S-P95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
S0095 (human, Caucasian) - GGB
S1391 (human, Caucasian) - GGB
S1887 (human, Caucasian) - GGB
S2793 (human, Caucasian, multiple malformations) - GGB
SA87f (human, Caucasian, Down syndrome, mosaic) - GGB
SA88 (human, Caucasian) - GGB
SA88f (human, Caucasian, Fanconi anemia) - GGB
SGA96M (human, Caucasian) - GGB
SM96P (human, Caucasian) - GGB
SS92 (human, Caucasian, nanism) - GGB
SV3T3 (mouse, BALB/c) - GEICH
T-D94 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
T-F96 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
T-M95f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
T-R96f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
T2385 (human, Caucasian) - GGB
T2389 (human, Caucasian) - GGB
T84M (human, Caucasian) - GGB
TM90 (human, Caucasian, Down syndrome, mosaic) - GGB
V-D95f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
V1396 (human, Caucasian) - GGB
V91 (human, Caucasian) - GGB
VBA88Mf (human, Caucasian) - GGB
VG84 (human, Caucasian, hermaphroditism true) - GGB
VK-B 92f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
WF 2 (fish - Walley whole fry) - IZSBS
Z-C93f (human, Caucasian, trisomy 21 / Down syndrome) - GGB
Z85 (human, Caucasian) - GGB


For information, get in touch with:
IRCCS AOU San Martino IST,
c/o Centro Biotecnologie Avanzate, Torre D - Piano 2

Largo Rosanna Benzi, 10 - I-16132 Genova - Italy
Dott.ssa Assunta Manniello
Email: mariaassunta.manniello@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