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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, Caucasian


- 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

C-4 II (cervix, carcinoma, cervical) - ECACC
C-4I (cervix, carcinoma, cervical) - ECACC
C-B94 (amnion, Edwards' syndrome / trisomy 18) - GGB
C-B95 (fibroblast, trisomy 21 / Down syndrome) - GGB
C-C87a (amnion, Edwards' syndrome / trisomy 18) - GGB
C-C87f (fibroblast, Edwards' syndrome / trisomy 18) - GGB
C-C90 (amnion, trisomy 21 / Down syndrome) - GGB
C-C91 (amnion, Klinefelter syndrome) - GGB
C-C95 (amnion, cri du chat syndrome) - GGB
C-D92 (amnion) - GGB
C-E 92 (amnion, trisomy 21 / Down syndrome) - GGB
C-F89 (fibroblast, trisomy 21 / Down syndrome) - GGB
C-G86 (amnion, trisomy 21 / Down syndrome) - GGB
C-M87 (fibroblast) - GGB
C-M92 (fibroblast, trisomy 21 / Down syndrome) - GGB
C-N90 (amnion, trisomy 21 / Down syndrome) - GGB
C-N95 (fibroblast, trisomy 21 / Down syndrome) - GGB
C-S91a (amnion, trisomy 21 / Down syndrome) - GGB
C-S95 (amnion, chromosome aberration) - GGB
C0092 (amnion, D. Becker syndrome) - GGB
C0994IL2 (lymphocyte, chromosome aberration) - GGB
C1191f (fibroblast, trisomy 14) - GGB
C1191v (fibroblast, trisomy 14) - GGB
C1192 (fibroblast, trisomy 7) - GGB
C1195 (fibroblast, Edwards' syndrome / trisomy 18) - GGB
C1293 (fibroblast, trisomy 21 / Down syndrome) - GGB
C1294a (amnion) - GGB
C1294f (fibroblast) - GGB
C1595a (amnion) - GGB
C1595f (fibroblast) - GGB
C1PV (skin, fibroblast) - PVCGU
C211 (skin, cri du chat syndrome) - ECACC
C2PV (skin, fibroblast) - PVCGU
C33A (cervix, carcinoma) - ICLC
C3PV (skin, fibroblast) - PVCGU
C4PV (skin, fibroblast) - PVCGU
C5PV (skin, fibroblast) - PVCGU
C6PV (skin, fibroblast, porokeratosis of Mibelli) - PVCGU
C7PV (skin, fibroblast, photosensitivity) - PVCGU
C83 (fibroblast) - GGB
C86M (lymphocyte) - GGB
C86P (lymphocyte) - GGB
C87 (fibroblast) - GGB
C8PV (skin, fibroblast) - PVCGU
C91 (fibroblast, chromosome mosaic) - GGB
C92 (fibroblast, D. Becker syndrome) - GGB
C93 (fibroblast, Pallister Killian syndrome) - GGB
C96 (amnion, trisomy 21 / Down syndrome) - GGB
C9PV (skin, fibroblast) - PVCGU
Ca Ski (cervix, carcinoma, epidermoid) - ECACC
Ca Ski (cervix, carcinoma) - MIISA
Ca Ski (cervix, carcinoma) - MIISB
CA295 (lymphocyte) - GGB
CA95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
CA96 (lymphocyte, familial epylepsy) - GGB
CACO-2 (colon, adenocarcinoma) - DSMZ
CACO-2 (colon, adenocarcinoma) - ECACC
Caco-2 (colon, adenocarcinoma) - ICLC
Caco-2 (colon, adenocarcinoma) - IZSBS
Caco-2 (colon, adenocarcinoma) - MIECC
Caco-2 (colon, adenocarcinoma) - MIUFC
Caco-2 (colon, adenocarcinoma) - RMSTC
Caco-2 (colon, adenocarcinoma) - SPBIC
CAKI 2 (kidney, carcinoma) - ECACC
Caki-1 (kidney, carcinoma) - IZSBS
Caki-2 (kidney, carcinoma) - ICLC
Caki-2 (kidney, carcinoma) - IZSBS
CALU 1 (lung, carcinoma, epidermoid) - ECACC
Calu-1 (lung, carcinoma, epidermoid, grade III) - ICLC
CaLu-1 (lung, carcinoma, epidermoid) - IZSBS
Calu-3 (lung, adenocarcinoma) - GEUEM
Calu-3 (lung, adenocarcinoma) - IZSBS
Calu-3 (lung, adenocarcinoma) - MIISB
Calu-6 (lung, adenocarcinoma) - GEUEM
Calu-6 (lung, carcinoma, anaplastic) - ICLC
CAPAN 1 (pancreas, adenocarcinoma) - IZSBS
CAPAN 2 (pancreas, carcinoma) - IZSBS
CAPAN-1 (pancreas, adenocarcinoma) - DSMZ
CAPAN-2 (pancreas, adenocarcinoma) - DSMZ
Capan-2 (pancreas, adenocarcinoma) - SPBIC
CaSki (cervix, carcinoma, epidermoid, from metastatic site) - ICLC
CC96 (lymphocyte, neurofibromatosis type I) - GGB
CCD 16Lu (lung) - ECACC
CCD 19Lu (lung) - ECACC
CCD 25Lu (lung) - ECACC
CCD 8Lu (lung) - ECACC
CCD-32Lu (lung) - ECACC
CCD-33Lu (lung) - ECACC
CCD-37Lu (lung) - ECACC
CCD-39Lu (lung) - ECACC
CCF-STTG1 (brain, astrocytoma) - ECACC
CCF-STTG1 (astrocytoma, anaplastic, grade IV) - IZSBS
CCM89M (lymphocyte) - GGB
CCRF-CEM (peripheral blood, leukemia, acute lymphoblastic) - ECACC
CCRF-CEM (peripheral blood, leukemia, acute lymphoblastic) - IZSBS
CCRF-CEM (peripheral blood, leukemia, acute lymphoblastic) - PSHTM
CCRF-HSB-2 (peripheral blood, leukemia, acute lymphoblastic T cell) - ECACC
CCRF-SB (peripheral blood, leukemia, acute lymphoblastic) - ECACC
CCRF-SB (peripheral blood, leukemia, acute lymphoblastic) - IZSBS
CCRF-SB (peripheral blood, leukemia, acute lymphoblastic) - SPBIC
CD88f (fibroblast, Down syndrome, mosaic) - GGB
CD88ls (lymphocyte, Down syndrome, mosaic) - GGB
CD89P (fibroblast) - GGB
CDM96 (lymphocyte, familial epylepsy) - GGB
CF84f (fibroblast, Down syndrome, mosaic) - GGB
CF84ls (lymphocyte, Down syndrome, mosaic) - GGB
CF89P (lymphocyte) - GGB
CF96F (lymphocyte) - GGB
CF96P (lymphocyte) - GGB
CFPAC-1 (pancreas, adenocarcinoma) - ECACC
CFPAC-1 (pancreas, adenocarcinoma, ductal) - ICLC
CG89 (lymphocyte, chromosome aberration) - GGB
CG94IL2 (lymphocyte, chromosome aberration) - GGB
CG96 (lymphocyte, neurofibromatosis type I) - GGB
Citrullinemia (skin, citrullinemia) - ECACC
CL95 (lymphocyte, trisomy 21 / Down syndrome) - GGB
CL96f (fibroblast, erythroblastopenia, transient) - GGB
CL96IL2 (lymphocyte, familial epylepsy) - GGB
CLM96M (lymphocyte) - GGB
Clone 15 HL-60 (leukemia, promyelocytic) - ECACC
CM-S/un (bone marrow, monocyte tumor) - ICLC
CM87 (lymphocyte, trisomy 21 / Down syndrome) - GGB
CM87IL2 (lymphocyte, trisomy 21 / Down syndrome) - GGB
CM88M (lymphocyte) - GGB
CM91IL2 (lymphocyte, chromosome aberration) - GGB
CM91ls (lymphocyte, Turner syndrome/noonan syndrome 1) - GGB
CM94 (lymphocyte) - GGB
CM94P (lymphocyte) - GGB
CMR94M (lymphocyte) - GGB
CN96 (lymphocyte) - GGB
COLO 201 (colon, adenocarcinoma) - ECACC
COLO 205 (colon, adenocarcinoma) - ECACC
COLO 205 (colon, colorectal adenocarcinoma) - ICLC
COLO 320DM (colon, adenocarcinoma) - ECACC
COLO 320HSR (colon, adenocarcinoma) - ECACC
COLO 320HSR (colon, adenocarcinoma) - SPBIC
COLO 839 (lymphocyte, B, melanoma) - ECACC
COLO-320 (colon, adenocarcinoma) - DSMZ
COLO-849 (melanoma, metastatic) - DSMZ
Cor Per (skin, fibroblast, Ehlers-Danlos syndrome, type IV, autosomal dominant) - BGEBS
COR-L105 (lung, adenocarcinoma) - ECACC
COR-L23 (lung, carcinoma, large cell) - ECACC
COR-L23 (lung, carcinoma, large cell) - ICLC
COR-L47 (bone marrow, carcinoma, lung small cell) - ECACC
COR-L51 (lung, carcinoma, lung small cell) - ECACC
COR-L88 (pleural effusion, carcinoma, lung small cell) - ECACC
CR83 (fibroblast, epidermolysis bullo'sa) - GGB
CR88P (lymphocyte) - GGB
CR96 (lymphocyte, epilepsy) - GGB
Cri du Chat (skin, fibroblast, cri du chat syndrome) - ECACC
CS191 (fibroblast, Turner syndrome, mosaic) - GGB
CS1PV (skin, fibroblast, Cockayne syndrome) - PVCGU
CS87 (lymphocyte, T, trisomy 21 / Down syndrome) - GGB
CS96 (fibroblast, Freeman-Sheldon syndrome) - GGB
CT96 (lymphocyte, hypercholesterolemia, familial) - GGB
CV96F (lymphocyte) - GGB
CVD89M (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