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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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GM02191
 
Resource Report
Resource Website 		Coriell Cat# GM02191, RRID:CVCL_1H59 Homo sapiens (Human) Huntington's disease Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. Finite cell line Female GM-2191 Coriell GM02191 CLO:CLO_0032264,
BioSample:SAMN00807600,
Coriell:GM02191,
Wikidata:Q54837368		 CVCL_1H59 2026-08-15 04:29:13 0
GM02295
 
Resource Report
Resource Website 		RRID:CVCL_4T29 Homo sapiens (Human) Winchester syndrome Population: Puerto Rican. PMID:22922033 Finite cell line Female GM-2295 CLO:CLO_0032204,
BioSample:SAMN00807665,
Coriell:GM02295,
Wikidata:Q54837411		 CVCL_4T29 2026-08-15 04:29:14 0
GM02317
 
Resource Report
Resource Website 		Coriell Cat# GM02317, RRID:CVCL_8A67 Homo sapiens (Human) Population: Caucasian; Irish. PMID:21418647
PMID:24555846
PMID:25326100 		Finite cell line Female GM-2317 Coriell GM02317 CLO:CLO_0032170,
BioSample:SAMN00807691,
Coriell:GM02317,
GEO:GSM651116,
GEO:GSM651117,
GEO:GSM1257698,
GEO:GSM1266973,
GEO:GSM1267052,
GEO:GSM1288440,
GEO:GSM1314048,
Wikidata:Q54837425		 CVCL_8A67 2026-08-15 04:29:14 0
GM02302
 
Resource Report
Resource Website 		RRID:CVCL_W226 Homo sapiens (Human) Hereditary coproporphyria Population: Caucasian. Transformed cell line Female GM-2302 CLO:CLO_0032201,
BioSample:SAMN00807673,
Coriell:GM02302,
Wikidata:Q54837416		 CVCL_W226 2026-08-15 04:29:14 0
GM02213
 
Resource Report
Resource Website 		RRID:CVCL_4J47 Homo sapiens (Human) Acute intermittent porphyria Population: Caucasian. Transformed cell line Female GM-2213 CLO:CLO_0032260,
BioSample:SAMN00807608,
Coriell:GM02213,
Wikidata:Q54837375		 CVCL_4J47 2026-08-15 04:29:13 0
GM02317
 
Resource Report
Resource Website 		RRID:CVCL_8A67 Homo sapiens (Human) Population: Caucasian; Irish. PMID:21418647
PMID:24555846
PMID:25326100 		Finite cell line Female GM-2317 CLO:CLO_0032170,
BioSample:SAMN00807691,
Coriell:GM02317,
GEO:GSM651116,
GEO:GSM651117,
GEO:GSM1257698,
GEO:GSM1266973,
GEO:GSM1267052,
GEO:GSM1288440,
GEO:GSM1314048,
Wikidata:Q54837425		 CVCL_8A67 2026-08-15 04:29:14 0
GM02268
 
Resource Report
Resource Website 		Coriell Cat# GM02268, RRID:CVCL_W662 Homo sapiens (Human) Hunter syndrome Population: Caucasian. Finite cell line Female GM-2268, GM02268A Coriell GM02268 CLO:CLO_0032121,
BioSample:SAMN00807646,
Coriell:GM02268,
Wikidata:Q54837400		 CVCL_W662 2026-08-15 04:29:13 0
GM02438
 
Resource Report
Resource Website 		Coriell Cat# GM02438, RRID:CVCL_IJ35 Homo sapiens (Human) Galactosialidosis PMID:8910459 Finite cell line Female GM02438A, GM02438a Coriell GM02438 CLO:CLO_0033286,
Coriell:GM02438,
Wikidata:Q54837490		 CVCL_IJ35 2026-08-15 04:29:16 0
GM02433
 
Resource Report
Resource Website 		RRID:CVCL_CZ14 Homo sapiens (Human) Population: Caucasian. Finite cell line Female CLO:CLO_0033284,
BioSample:SAMN00807769,
Coriell:GM02433,
Wikidata:Q54837485		 CVCL_CZ14 2026-08-15 04:29:15 0
GM02329
 
Resource Report
Resource Website 		Coriell Cat# GM02329, RRID:CVCL_X263 Homo sapiens (Human) Trisomy 9 Karyotypic information: 47,XX,+9 [5]; 46,XX [45] (Coriell=GM02329)., Population: Caucasian. PMID:6661932 Finite cell line Female GM-2329, GM 2329 Coriell GM02329 CLO:CLO_0033128,
BioSample:SAMN00807701,
Coriell:GM02329,
Wikidata:Q54837430		 CVCL_X263 2026-08-15 04:29:14 0
GM02442
 
Resource Report
Resource Website 		RRID:CVCL_GR98 Homo sapiens (Human) Type 1 diabetes mellitus Population: Native Central American; Pima. Finite cell line Female CLO:CLO_0033317,
BioSample:SAMN00807779,
Coriell:GM02442,
Wikidata:Q54837496		 CVCL_GR98 2026-08-15 04:29:16 0
GM02429
 
Resource Report
Resource Website
Discontinued 		RRID:CVCL_L974 Homo sapiens (Human) Homocystinuria Transformed cell line Female GM02375 CLO:CLO_0033094,
BioSample:SAMN00807761,
Coriell:GM02375,
Coriell:GM02429,
Wikidata:Q54837480		 CVCL_L974 2026-08-15 04:29:15 0
GM02337
 
Resource Report
Resource Website 		Coriell Cat# GM02337, RRID:CVCL_X090 Homo sapiens (Human) Cri du chat syndrome Karyotypic information: 46,XX,del(5)(qter->p14) (Coriell=GM02337)., Population: Caucasian. PMID:6617268
PMID:6661932 		Finite cell line Female GM-2337, GM 2337 Coriell GM02337 CLO:CLO_0033122,
BioSample:SAMN00807717,
Coriell:GM02337,
Wikidata:Q54837438		 CVCL_X090 2026-08-15 04:29:14 0
GM02355
 
Resource Report
Resource Website 		RRID:CVCL_L945 Homo sapiens (Human) Familial adenomatous polyposis Population: Caucasian. Finite cell line Female GM2355 CLO:CLO_0033110,
BioSample:SAMN00807733,
Coriell:GM02355,
Wikidata:Q54837455		 CVCL_L945 2026-08-15 04:29:15 0
GM02430
 
Resource Report
Resource Website 		Coriell Cat# GM17321, RRID:CVCL_M996 Homo sapiens (Human) Transformed cell line Female GM17321 Coriell GM17321 CLO:CLO_0013646,
CLO:CLO_0033274,
BioSample:SAMN00807763,
Coriell:GM02430,
Coriell:GM17321,
Wikidata:Q54837481		 CVCL_M996 2026-08-15 04:29:15 0
GM02347
 
Resource Report
Resource Website 		Coriell Cat# GM02347, RRID:CVCL_1U23 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Transformed cell line Female GM-2347 Coriell GM02347 CLO:CLO_0033109,
BioSample:SAMN00807731,
Coriell:GM02347,
Wikidata:Q54837454		 CVCL_1U23 2026-08-15 04:29:15 0
GM02351
 
Resource Report
Resource Website 		Coriell Cat# GM02351, RRID:CVCL_B5LN Homo sapiens (Human) Farber lipogranulomatosis PMID:9458280 Finite cell line Female GM 02351 Coriell GM02351 Coriell:GM02351,
Wikidata:Q111733237		 CVCL_B5LN 2026-08-15 04:29:15 0
GM02446
 
Resource Report
Resource Website 		RRID:CVCL_D862 Homo sapiens (Human) Adenosine deaminase deficiency Population: Hispanic. PMID:7380831 Finite cell line Female GM-2446, GM 2446 CLO:CLO_0033319,
BioSample:SAMN00807783,
Coriell:GM02446,
Wikidata:Q54837498		 CVCL_D862 2026-08-15 04:29:16 0
GM02351
 
Resource Report
Resource Website 		RRID:CVCL_B5LN Homo sapiens (Human) Farber lipogranulomatosis PMID:9458280 Finite cell line Female GM 02351 Coriell:GM02351,
Wikidata:Q111733237		 CVCL_B5LN 2026-08-15 04:29:15 0
GM02347
 
Resource Report
Resource Website 		RRID:CVCL_1U23 Homo sapiens (Human) Autosomal dominant torsion dystonia 1 Transformed cell line Female GM-2347 CLO:CLO_0033109,
BioSample:SAMN00807731,
Coriell:GM02347,
Wikidata:Q54837454		 CVCL_1U23 2026-08-15 04:29:15 0

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