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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: amnion


- 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

A-B92a (human, Caucasian) - GGB
A-C88 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
A-P92 (human, Caucasian) - GGB
A-S91 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
AV 3 (human) - IZSBS
AV3 (human) - ECACC
B-A95 (human, Caucasian) - GGB
B-B87 (human, Caucasian) - GGB
B-B88a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B-C86 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B-C89 (human, Caucasian) - GGB
B-D93 (human, Caucasian, Down syndrome, mosaic) - GGB
B-DP85 (human, trisomy 21 / Down syndrome) - GGB
B-F91 (human, Caucasian, Patau syndrome / trisomy 13) - GGB
B-G92 (human, Caucasian, Turner syndrome, mosaic) - GGB
B-K88 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B-L94 (human, Caucasian) - GGB
B-M 92a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B-M91a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B-M93 (human, Caucasian) - GGB
B-P91 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
B-P94 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B-R92 (human, Caucasian, chromosome aberration) - GGB
B-R93a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B-S95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
B-V92 (human, Caucasian) - GGB
B-Z94 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
C-B94 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
C-C87a (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
C-C90 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
C-C91 (human, Caucasian, Klinefelter syndrome) - GGB
C-C95 (human, Caucasian, cri du chat syndrome) - GGB
C-D92 (human, Caucasian) - GGB
C-E 92 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
C-G86 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
C-N90 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
C-S91a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
C-S95 (human, Caucasian, chromosome aberration) - GGB
C0092 (human, Caucasian, D. Becker syndrome) - GGB
C1294a (human, Caucasian) - GGB
C1595a (human, Caucasian) - GGB
C96 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
D-A92a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
D-B87 (human, Caucasian) - GGB
D-C95 (human, Caucasian) - GGB
D-F94 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
D-M89 (human, Caucasian, Patau syndrome / trisomy 13) - GGB
D-R86 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
D-T93 (human, Caucasian) - GGB
DB-R95 (human, Caucasian) - GGB
DC-P87 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
DP-LL95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
E-P95 (human, Caucasian, Meckel syndrome) - GGB
ES-095 (human, Caucasian) - GGB
F-C87 (human, Caucasian) - GGB
F-D96 (human, Caucasian) - GGB
F-M91 (human, Caucasian) - GGB
F-M96 (human, Caucasian) - GGB
F-P89 (human, Caucasian) - GGB
F-P96 (human, Caucasian, anencephaly) - GGB
FL (human) - ECACC
FL (human) - IZSBS
FL (human) - MWIIW
G-A88 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
G-B90 (human, Caucasian) - GGB
G-C195 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
G-C92 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
G-C95 (human, Caucasian, anencephaly) - GGB
G-F92a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
G-F95 (human, Caucasian) - GGB
G-M89 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
G-M95a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
H-A88 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
I-B92 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
I-P94 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
IGA001/83 (human, Caucasian) - GEIMM
IGA001/85 (human, Caucasian, propionicacidemia I) - GEIMM
IGA001/92 (human, Caucasian, maple syrup urine disease) - GEIMM
IGA001/99 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGA004/90 (human, Caucasian, glycogen storage disease II) - GEIMM
IGA004/95 (human, Caucasian, Krabbe disease) - GEIMM
IGA004/99 (human, Caucasian, methylmalonicacidemia) - GEIMM
IGA005/84 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA005/98 (human, Caucasian, methylmalonicacidemia) - GEIMM
IGA007/96 (human, Caucasian, mucolipidosis II) - GEIMM
IGA008/82 (human, Caucasian, glycogen storage disease II) - GEIMM
IGA009/84 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGA009/98 (human, Caucasian, mucolipidosis II) - GEIMM
IGA010/89 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGA013/83 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA015/96 (human, Caucasian, galactosemia) - GEIMM
IGA016/84 (human, Caucasian, cystinosis, early-onset or infantile nephropathic type) - GEIMM
IGA017/99 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA018/85 (human, Caucasian, Tay-Sachs disease) - GEIMM
IGA020/90 (human, Caucasian, metachromatic leukodystrophy, late-infantile) - GEIMM
IGA022/82 (human, Caucasian, fucosidosis) - GEIMM
IGA022/99 (human, Caucasian, Menkes syndrome) - GEIMM
IGA024/90 (human, Caucasian, Niemann-Pick disease, type A) - GEIMM
IGA028/83 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA031/82 (human, Caucasian, glycogen storage disease II) - GEIMM
IGA031/87 (human, Caucasian) - GEIMM
IGA033/83 (human, Caucasian, mucopolysaccharidosis type I / Hurler disease) - GEIMM
IGA036/83 (human, Caucasian, glycogen storage disease II) - GEIMM
IGA040/78 (human, Caucasian, fucosidosis) - GEIMM
IGA040/82 (human, Caucasian, propionicacidemia I) - GEIMM
IGA058/80 (human, Caucasian, glycogen storage disease II) - GEIMM
IGA063/80 (human, Caucasian, mucopolysaccharidosis type VI) - GEIMM
IGA188/78 (human, Caucasian, mannosidosis, alpha b, lysosomal) - GEIMM
L-A86 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
L-C90 (human, Caucasian, hydrocephalus) - GGB
L-DR92a (human, Caucasian, chromosome aberration) - GGB
L-F95 (human, Caucasian) - GGB
L-M92 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
L-V91 (human, Caucasian, Miller-Dieker syndrome) - GGB
L-V94 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
L-Z93a (human, Caucasian, chromosome aberration) - GGB
LM-M92 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-B87a (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
M-B95a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-C95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-F92 (human, Caucasian, Patau syndrome / trisomy 13) - GGB
M-G93 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-L95a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-M96 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-N91 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-P88 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
M-P91a (human, Caucasian, Fanconi anemia) - GGB
M-R95 (human, Caucasian) - GGB
M-T95a (human, Caucasian) - GGB
N-A90 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
N-B88 (human, Caucasian) - GGB
N-C96 (human, Caucasian, Patau syndrome / trisomy 13) - GGB
O-B94a (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
O-C94 (human, Caucasian, tetraphocomelia) - GGB
P-190 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
P-B88 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
P-B91 (human, Caucasian, chromosome aberration) - GGB
P-B92 (human, Caucasian, chromosome aberration) - GGB
P-C96 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
P-D89 (human, Caucasian) - GGB
P-D91 (human, Caucasian) - GGB
P-D94a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
P-G96 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
P-L92 (human, Caucasian, chromosome aberration) - GGB
P-NC94 (human, Caucasian) - GGB
P-R90 (human, Caucasian) - GGB
P-S96 (human, Caucasian) - GGB
P1985a (human, Caucasian, chondrodysplasia) - GGB
P1985f (human, Caucasian, chondrodysplasia) - GGB
P92 (human, Caucasian, Prune Belly syndrome) - GGB
P93 (human, Caucasian, Turner syndrome/noonan syndrome 1) - GGB
P95 (human, Caucasian, Apert syndrome) - GGB
PS192 (human, Caucasian, Prune Belly syndrome) - GGB
QV-R94 (human, Caucasian, anencephaly) - GGB
R-B92 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
R-C95a (human, Caucasian, Patau syndrome / trisomy 13) - GGB
R-C96 (human, Caucasian) - GGB
R-DC90a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
R-G196 (human, Caucasian) - GGB
R-G94a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
R-M94 (human, Caucasian) - GGB
R-M95 (human, Caucasian) - GGB
R-P 91a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
R-R92 (human, Caucasian) - GGB
R-T96 (human, Caucasian) - GGB
R95 (human, Caucasian) - GGB
S-C88 (human, Caucasian, omphalocele) - GGB
S-C93 (human, Caucasian) - GGB
S-D92a (human, Caucasian, Turner syndrome/noonan syndrome 1) - GGB
S-G87 (human, Caucasian) - GGB
S-L90a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
S-L95a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
S-N87 (human, Caucasian) - GGB
S-R96 (human, Caucasian) - GGB
S-T92a (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
S-T92f (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
T-C90 (human, Caucasian) - GGB
T-G88 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
T-M95a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
T-P90 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
T-P92 (human, Caucasian, chromosome aberration) - GGB
T-P92I (human, Caucasian) - GGB
T-P92II (human, Caucasian) - GGB
T-R96a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
T-S90 (human, Caucasian) - GGB
T93 (human, Caucasian, Edwards' syndrome / trisomy 18) - GGB
U (human) - MWIIW
V-B95 (human, Caucasian, trisomy 21 / Down syndrome) - GGB
V-C89a (human, Caucasian) - GGB
V-C91 (human, Caucasian) - GGB
V-C92 (human, Caucasian, chromosome aberration) - GGB
V-D95a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
V-M88 (human, Caucasian) - GGB
VK-B 92a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
WISH (human) - ECACC
WISH (human) - IZSBS
WISH (human) - RMUVI
WISH (human) - SIUCC
Z-C93a (human, Caucasian, trisomy 21 / Down syndrome) - GGB
Z-M94 (human, Caucasian) - 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