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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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95,747 Results - per page

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GM03639
 
Resource Report
Resource Website 		RRID:CVCL_F188 Homo sapiens (Human) Childhood T acute lymphoblastic leukemia PMID:62390
PMID:2144611
PMID:8547074 		Cancer cell line Female GM03639A, GM03639C, T cell line 8402, 8402 CLO:CLO_0017159,
Coriell:GM03639,
Cosmic:2361363,
IARC_TP53:21652,
Wikidata:Q54838168		 CVCL_F188 2026-08-15 04:29:32 0
GM03691
 
Resource Report
Resource Website 		RRID:CVCL_U394 Homo sapiens (Human) Tay-Sachs disease Transformed cell line Female CLO:CLO_0015481,
BioSample:SAMN00808498,
Coriell:GM03691,
Wikidata:Q54838193		 CVCL_U394 2026-08-15 04:29:33 0
GM03643
 
Resource Report
Resource Website 		RRID:CVCL_V043 Homo sapiens (Human) Huntington's disease Population: Caucasian. Transformed cell line Female GM3643 CLO:CLO_0017150,
BioSample:SAMN00808480,
Coriell:GM03643,
Wikidata:Q54838172		 CVCL_V043 2026-08-15 04:29:33 0
GM03625
 
Resource Report
Resource Website 		RRID:CVCL_2Y87 Homo sapiens (Human) Cartilage hair hypoplasia Population: Caucasian; Amish. Finite cell line Female GM03625B CLO:CLO_0017205,
BioSample:SAMN00808475,
Coriell:GM03625,
Wikidata:Q54838165		 CVCL_2Y87 2026-08-15 04:29:32 0
GM03723
 
Resource Report
Resource Website 		RRID:CVCL_X453 Homo sapiens (Human) Maroteaux-Lamy syndrome Population: African American. Transformed cell line Female CLO:CLO_0015469,
BioSample:SAMN00808509,
Coriell:GM03723,
Wikidata:Q54838208		 CVCL_X453 2026-08-15 04:29:34 0
GM03655
 
Resource Report
Resource Website 		RRID:CVCL_V250 Bos taurus (Bovine) Finite cell line Female GM3655 CLO:CLO_0015444,
Coriell:GM03655,
Wikidata:Q54838181		 CVCL_V250 2026-08-15 04:29:33 0
GM03641
 
Resource Report
Resource Website
Possibly Discontinued 		Coriell Cat# AG03641, RRID:CVCL_DF21 Homo sapiens (Human) Retinoblastoma PMID:7253718 Transformed cell line Female AG03641, AG3641 Coriell AG03641 CLO:CLO_0017162,
BioSample:SAMN00808478,
Coriell:AG03641,
Coriell:GM03641,
Wikidata:Q54838170		 CVCL_DF21 2026-08-15 04:29:33 0
GM03715
 
Resource Report
Resource Website 		RRID:CVCL_7401 Homo sapiens (Human) Population: Caucasian; Northern European., Part of: Human variation panel. PMID:11416159 Transformed cell line Female GM17001 CLO:CLO_0015460,
CLO:CLO_0018044,
BioSample:SAMN00808503,
Coriell:GM03715,
Coriell:GM17001,
Wikidata:Q54838202		 CVCL_7401 2026-08-15 04:29:34 0
GM03714
 
Resource Report
Resource Website
1+ mentions 		Coriell Cat# GM03714, RRID:CVCL_7400 Homo sapiens (Human) PMID:17668376
PMID:23943852 		Transformed cell line Female GM03714A Coriell GM03714 CLO:CLO_0015457,
BioSample:SAMN00808502,
Coriell:GM03714,
GEO:GSM1116593,
GEO:GSM1116594,
GEO:GSM1116595,
GEO:GSM1116596,
Wikidata:Q54838201		 CVCL_7400 2026-08-15 04:29:34 1
GM03721
 
Resource Report
Resource Website 		Coriell Cat# GM03721, RRID:CVCL_M941 Homo sapiens (Human) Population: African American., Part of: Human variation panel. Transformed cell line Female GM17157 Coriell GM03721 CLO:CLO_0013962,
CLO:CLO_0015467,
BioSample:SAMN00808507,
Coriell:GM03721,
Coriell:GM17157,
GEO:GSM273424,
GEO:GSM569659,
GEO:GSM596222,
GEO:GSM597022,
GEO:GSM924667,
Wikidata:Q54838206		 CVCL_M941 2026-08-15 04:29:34 0
GM03650
 
Resource Report
Resource Website 		RRID:CVCL_AB33 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0015447,
BioSample:SAMN00808485,
Coriell:GM03650,
Wikidata:Q54838177		 CVCL_AB33 2026-08-15 04:29:33 0
GM03606
 
Resource Report
Resource Website 		RRID:CVCL_V471 Homo sapiens (Human) Down syndrome Finite cell line Female CLO:CLO_0017226,
BioSample:SAMN00808469,
Coriell:GM03606,
Wikidata:Q54838156		 CVCL_V471 2026-08-15 04:29:32 0
GM03640
 
Resource Report
Resource Website
Possibly Discontinued 		Coriell Cat# GM03640, RRID:CVCL_DF20 Homo sapiens (Human) Retinoblastoma PMID:7253718 Transformed cell line Female AG03640, AG3640 Coriell GM03640 CLO:CLO_0017161,
BioSample:SAMN00808477,
Coriell:AG03640,
Coriell:GM03640,
Wikidata:Q54838169		 CVCL_DF20 2026-08-15 04:29:33 0
GM03714
 
Resource Report
Resource Website
1+ mentions 		RRID:CVCL_7400 Homo sapiens (Human) PMID:17668376
PMID:23943852 		Transformed cell line Female GM03714A CLO:CLO_0015457,
BioSample:SAMN00808502,
Coriell:GM03714,
GEO:GSM1116593,
GEO:GSM1116594,
GEO:GSM1116595,
GEO:GSM1116596,
Wikidata:Q54838201		 CVCL_7400 2026-08-15 04:29:34 1
GM03722
 
Resource Report
Resource Website 		Coriell Cat# GM03722, RRID:CVCL_X452 Homo sapiens (Human) Maroteaux-Lamy syndrome Population: African American. Finite cell line Female Coriell GM03722 CLO:CLO_0015465,
BioSample:SAMN00808508,
Coriell:GM03722,
Wikidata:Q54838207		 CVCL_X452 2026-08-15 04:29:34 0
GM03833
 
Resource Report
Resource Website 		Coriell Cat# GM03833, RRID:CVCL_AK84 Homo sapiens (Human) Retinitis pigmentosa Population: Caucasian. Finite cell line Female Coriell GM03833 CLO:CLO_0015663,
BioSample:SAMN00808557,
Coriell:GM03833,
Wikidata:Q54838261		 CVCL_AK84 2026-08-15 04:29:36 0
GM03790
 
Resource Report
Resource Website 		RRID:CVCL_1H64 Homo sapiens (Human) Huntington's disease Transformed cell line Female CLO:CLO_0015569,
BioSample:SAMN00808535,
Coriell:GM03790,
Wikidata:Q54838239		 CVCL_1H64 2026-08-15 04:29:35 0
GM03816
 
Resource Report
Resource Website
1+ mentions 		RRID:CVCL_F193 Homo sapiens (Human) Friedreich ataxia Population: Caucasian. PMID:28444186 Finite cell line Female GM-3816 CLO:CLO_0015531,
BioSample:SAMN00808548,
Coriell:GM03816,
Wikidata:Q54838252		 CVCL_F193 2026-08-15 04:29:36 1
GM03723
 
Resource Report
Resource Website 		Coriell Cat# GM03723, RRID:CVCL_X453 Homo sapiens (Human) Maroteaux-Lamy syndrome Population: African American. Transformed cell line Female Coriell GM03723 CLO:CLO_0015469,
BioSample:SAMN00808509,
Coriell:GM03723,
Wikidata:Q54838208		 CVCL_X453 2026-08-15 04:29:34 0
GM03786
 
Resource Report
Resource Website 		RRID:CVCL_N012 Homo sapiens (Human) Karyotypic information: 45,XX,dic(13;14)(13qter->13p11::14p11->14qter) (Coriell=GM03786)., Population: Caucasian; Greek., Part of: Human variation panel. Finite cell line Female GM17375 CLO:CLO_0013696,
CLO:CLO_0015567,
BioSample:SAMN00808534,
Coriell:GM03786,
Coriell:GM17375,
Wikidata:Q54838238		 CVCL_N012 2026-08-15 04:29:35 0

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