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Cellosaurus is database indexing available cell lines from various collections: American Type Culture Collection (ATCC), Bioresource Collection and Research Center, Taiwan (BCRC), Banco de Células do Rio de Janeiro (BCRJ), CellBank Australia (CBA), Collection of Cell Lines in Veterinary Medicine (CCLV), Cell Lines Service (CLS), Coriell, Drosophila Genomics Resource Center (DGRC), Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ), European Bank for induced pluripotent Stem Cells (EBiSC), European Collection of Authenticated Cell Cultures (ECACC), Interlab Cell Line Collection (ICLC), Institute for Fermentation Osaka (IFO), Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna (IZSLER) biobank, Japanese Collection of Research Bioresources (JCRB) Cell Bank, Kunming Cell Bank of Type Culture Collection (KCB), Korean Cell Line Bank (KCLB), Millipore, National Cell Bank of Iran (NCBI_Iran), National Cancer Institute - Developmental Therapeutics Program (NCI-DTP), NINDS Human Cell and Data Repository (NHCDR), NIH AIDS Reagent Program (NIH-ARP), NISES, RIKEN Bioresource Center Cell Bank (RCB), Royan Stem Cell Bank (RSCB), Tick Cell Biobank (TCB), Tohoku University cell line catalog (TKG), and Ximbio.

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GM02047
 
Resource Report
Resource Website 		RRID:CVCL_L762 Homo sapiens (Human) Population: Caucasian. PMID:16465621 Finite cell line Male GM-2047 CLO:CLO_0032558,
BioSample:SAMN00807424,
Coriell:GM02047,
Wikidata:Q54837262		 CVCL_L762 Cellosaurus 2026-09-26 06:48:52 0
GM02052+hTERT
 
Resource Report
Resource Website 		RRID:CVCL_VL09 Homo sapiens (Human) Ataxia telangiectasia syndrome Population: Jewish; Moroccan. PMID:11313956 Telomerase immortalized cell line Female hTERT+ GM02052 Wikidata:Q93575552 cvcl_7350 CVCL_VL09 Cellosaurus 2026-09-26 06:48:52 0
GM02037
 
Resource Report
Resource Website
1+ mentions 		RRID:CVCL_7349 Homo sapiens (Human) Karyotypic information: 46,XY [45]; 46,XY,t(4;16)(4qter->4p14::16q24->16qter;16pter->16q24::4p14->4pter) [5] (Coriell=GM02037)., Population: Caucasian. PMID:6223188
PMID:8643543
PMID:30567591 		Finite cell line Male GM2037, GM-2037, GM 2037, GM02037A, GM2037A, GM 2037A, GM02037B, GM 2037B, GM02037C BTO:BTO_0003842,
CLO:CLO_0032574,
BioSample:SAMN00807416,
Coriell:GM02037,
GEO:GSM3124641,
Wikidata:Q54837256		 CVCL_7349 Cellosaurus 2026-09-26 06:48:51 1
GM02074
 
Resource Report
Resource Website 		RRID:CVCL_0P00 Homo sapiens (Human) Population: African American. Finite cell line Female GM-2074 CLO:CLO_0032512,
BioSample:SAMN00807460,
Coriell:GM02074,
Wikidata:Q54837287		 CVCL_0P00 Cellosaurus 2026-09-26 06:48:52 0
GM02017
 
Resource Report
Resource Website 		RRID:CVCL_M992 Homo sapiens (Human) Population: Arab., Part of: Human variation panel. PMID:8328452 Finite cell line Male GM-2017, GM 02017, GM17333 CLO:CLO_0013617,
CLO:CLO_0032316,
BioSample:SAMN00807392,
Coriell:GM02017,
Coriell:GM17333,
Wikidata:Q54837240		 CVCL_M992 Cellosaurus 2026-09-26 06:48:51 0
GM02038
 
Resource Report
Resource Website 		Coriell Cat# GM02038, RRID:CVCL_CW68 Homo sapiens (Human) Schizophrenia Population: Caucasian. PMID:7847674
PMID:21490598 		Finite cell line Male GM-2038 Coriell GM02038 CLO:CLO_0032554,
BioSample:SAMN00807418,
Coriell:GM02038,
Wikidata:Q54837257		 CVCL_CW68 Cellosaurus 2026-09-26 06:48:51 0
GM02121
 
Resource Report
Resource Website
Possibly Discontinued 		Coriell Cat# GM02121, RRID:CVCL_JB66 Homo sapiens (Human) Finite cell line Female GM-2121 Coriell GM02121 Coriell:GM02121,
Wikidata:Q54837306		 CVCL_JB66 Cellosaurus 2026-09-26 06:48:52 0
GM02054
 
Resource Report
Resource Website 		RRID:CVCL_X087 Homo sapiens (Human) PMID:6617268
PMID:6661932 		Transformed cell line Male GM-2054, GM 2054 CLO:CLO_0032538,
BioSample:SAMN00807438,
Coriell:GM02054,
Wikidata:Q54837273		 CVCL_X087 Cellosaurus 2026-09-26 06:48:52 0
GM02055
 
Resource Report
Resource Website 		Coriell Cat# GM02055, RRID:CVCL_H177 Homo sapiens (Human) PMID:6617268 Finite cell line Female GM-2055, GM 2055 Coriell GM02055 CLO:CLO_0032535,
Coriell:GM02055,
Wikidata:Q54837274		 CVCL_H177 Cellosaurus 2026-09-26 06:48:52 0
GM02110
 
Resource Report
Resource Website
Discontinued 		Coriell Cat# GM01450, RRID:CVCL_L962 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Transformed cell line Male GM-2110, GM02110A, GM01450, GM-1450 Coriell GM01450 CLO:CLO_0031830,
BioSample:SAMN00807494,
Coriell:GM01450,
Coriell:GM02110,
Wikidata:Q54837305		 CVCL_L962 Cellosaurus 2026-09-26 06:48:52 0
GM02110
 
Resource Report
Resource Website
Discontinued 		RRID:CVCL_L962 Homo sapiens (Human) Hyperlipoproteinemia, type IIa Transformed cell line Male GM-2110, GM02110A, GM01450, GM-1450 CLO:CLO_0031830,
BioSample:SAMN00807494,
Coriell:GM01450,
Coriell:GM02110,
Wikidata:Q54837305		 CVCL_L962 Cellosaurus 2026-09-26 06:48:52 0
GM02028
 
Resource Report
Resource Website 		RRID:CVCL_CZ13 Homo sapiens (Human) Finite cell line Male GM-2028, GM02028A CLO:CLO_0032575,
Coriell:GM02028,
Wikidata:Q54837247		 CVCL_CZ13 Cellosaurus 2026-09-26 06:48:51 0
GM02121
 
Resource Report
Resource Website
Possibly Discontinued 		RRID:CVCL_JB66 Homo sapiens (Human) Finite cell line Female GM-2121 Coriell:GM02121,
Wikidata:Q54837306		 CVCL_JB66 Cellosaurus 2026-09-26 06:48:52 0
GM02046
 
Resource Report
Resource Website 		RRID:CVCL_L761 Homo sapiens (Human) Population: Caucasian. PMID:16465621 Finite cell line Female GM-2046 CLO:CLO_0032557,
BioSample:SAMN00807422,
Coriell:GM02046,
Wikidata:Q54837261		 CVCL_L761 Cellosaurus 2026-09-26 06:48:52 0
GM02027
 
Resource Report
Resource Website
Possibly Discontinued 		Coriell Cat# GM02027, RRID:CVCL_JB69 Homo sapiens (Human) Finite cell line Female GM-2027 Coriell GM02027 Coriell:GM02027,
Wikidata:Q54837246		 CVCL_JB69 Cellosaurus 2026-09-26 06:48:51 0
GM02052A-hTERT
 
Resource Report
Resource Website 		RRID:CVCL_VL04 Homo sapiens (Human) Ataxia telangiectasia syndrome Population: Jewish; Moroccan. PMID:12446774
PMID:21149446 		Telomerase immortalized cell line Female GM02052A-hTert Wikidata:Q93575554 cvcl_7350 CVCL_VL04 Cellosaurus 2026-09-26 06:48:52 0
GM02077
 
Resource Report
Resource Website 		RRID:CVCL_1H39 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at 50% risk for disease., Population: Caucasian. Finite cell line Female GM-2077 CLO:CLO_0032514,
BioSample:SAMN00807464,
Coriell:GM02077,
Wikidata:Q54837289		 CVCL_1H39 Cellosaurus 2026-09-26 06:48:52 0
GM02049
 
Resource Report
Resource Website 		RRID:CVCL_AB44 Homo sapiens (Human) Population: Arab. Finite cell line Male GM-2049 CLO:CLO_0032550,
BioSample:SAMN00807428,
Coriell:GM02049,
Wikidata:Q54837265		 CVCL_AB44 Cellosaurus 2026-09-26 06:48:52 0
GM02045
 
Resource Report
Resource Website
Possibly Discontinued 		Coriell Cat# GM02045, RRID:CVCL_CX28 Homo sapiens (Human) I-cell disease Finite cell line Male GM-2045 Coriell GM02045 Coriell:GM02045,
Wikidata:Q54837260		 CVCL_CX28 Cellosaurus 2026-09-26 06:48:52 0
GM02063
 
Resource Report
Resource Website
Possibly Discontinued
Possibly Discontinued 		Coriell Cat# GM00177, RRID:CVCL_F127 Homo sapiens (Human) Lesch-Nyhan syndrome Population: African American. PMID:180603 Finite cell line Male LN, GM-2063, GM 2063, GM-02063, GM00177, GM 177, GM-177, GM177 Coriell GM00177 Coriell:GM00177,
Coriell:GM02063,
Wikidata:Q54837280		 CVCL_F127 Cellosaurus 2026-09-26 06:48:52 0

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