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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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GM22031
 
Resource Report
Resource Website 		RRID:CVCL_5R49 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male Coriell:GM22031,
Wikidata:Q54852309		 CVCL_5R49 2026-02-07 08:10:39 0
GM22032
 
Resource Report
Resource Website 		Coriell Cat# GM22032, RRID:CVCL_5R50 Homo sapiens (Human) Azoospermia PMID:23665875 Transformed cell line Male Coriell GM22032 CLO:CLO_0014824,
Coriell:GM22032,
Wikidata:Q54852310		 CVCL_5R50 2026-02-07 08:10:39 0
GM22049
 
Resource Report
Resource Website 		RRID:CVCL_5R51 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Male Coriell:GM22049,
Wikidata:Q54852314		 CVCL_5R51 2026-02-07 08:10:29 0
GM22122
 
Resource Report
Resource Website 		Coriell Cat# GM22122, RRID:CVCL_5R53 Homo sapiens (Human) PMID:23665875 Finite cell line Male Coriell GM22122 Coriell:GM22122,
Wikidata:Q54852360		 CVCL_5R53 2026-02-07 08:10:31 0
GM22364
 
Resource Report
Resource Website 		Coriell Cat# GM22364, RRID:CVCL_5R61 Homo sapiens (Human) Chromosome 15q11-q13 duplication syndrome PMID:23495136
PMID:23665875 		Transformed cell line Male 801-005 LCL Coriell GM22364 Coriell:GM22364,
Wikidata:Q54852542		 CVCL_5R61 2026-02-07 08:10:42 0
GM22478
 
Resource Report
Resource Website 		RRID:CVCL_5M63 Homo sapiens (Human) Jacobsen syndrome Karyotypic information: 46,XX,del(11)(pter->q24.1) (Coriell=GM22478). PMID:23665875 Transformed cell line Female Coriell:GM22478,
Wikidata:Q54852569		 CVCL_5M63 2026-02-07 08:10:42 0
GM22397
 
Resource Report
Resource Website 		Coriell Cat# GM22397, RRID:CVCL_5R66 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Male Coriell GM22397 Coriell:GM22397,
Wikidata:Q54852564		 CVCL_5R66 2026-02-07 08:10:36 0
GM22478
 
Resource Report
Resource Website 		Coriell Cat# GM22478, RRID:CVCL_5M63 Homo sapiens (Human) Jacobsen syndrome Karyotypic information: 46,XX,del(11)(pter->q24.1) (Coriell=GM22478). PMID:23665875 Transformed cell line Female Coriell GM22478 Coriell:GM22478,
Wikidata:Q54852569		 CVCL_5M63 2026-02-07 08:10:36 0
GM22475
 
Resource Report
Resource Website 		Coriell Cat# GM22475, RRID:CVCL_5M62 Homo sapiens (Human) Jacobsen syndrome PMID:23665875 Transformed cell line Female Coriell GM22475 Coriell:GM22475,
Wikidata:Q54852568		 CVCL_5M62 2026-02-07 08:10:36 0
GM22421
 
Resource Report
Resource Website 		Coriell Cat# GM22421, RRID:CVCL_5M60 Homo sapiens (Human) Jacobsen syndrome PMID:23665875 Transformed cell line Male Coriell GM22421 Coriell:GM22421,
Wikidata:Q54852566		 CVCL_5M60 2026-02-07 08:10:36 0
GM22439
 
Resource Report
Resource Website 		RRID:CVCL_5M61 Homo sapiens (Human) Jacobsen syndrome PMID:23665875 Transformed cell line Female Coriell:GM22439,
Wikidata:Q54852567		 CVCL_5M61 2026-02-07 08:10:36 0
GM22397
 
Resource Report
Resource Website 		RRID:CVCL_5R66 Homo sapiens (Human) Autism spectrum disorder PMID:23665875 Transformed cell line Male Coriell:GM22397,
Wikidata:Q54852564		 CVCL_5R66 2026-02-07 08:10:36 0
GM22475
 
Resource Report
Resource Website 		RRID:CVCL_5M62 Homo sapiens (Human) Jacobsen syndrome PMID:23665875 Transformed cell line Female Coriell:GM22475,
Wikidata:Q54852568		 CVCL_5M62 2026-02-07 08:10:36 0
GM22629
 
Resource Report
Resource Website 		RRID:CVCL_1K42 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Female Coriell:GM22629,
Wikidata:Q54852670		 CVCL_1K42 2026-02-07 08:10:39 0
GM22594
 
Resource Report
Resource Website 		Coriell Cat# GM22594, RRID:CVCL_5R87 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM22594 Coriell:GM22594,
Wikidata:Q54852643		 CVCL_5R87 2026-02-07 08:10:38 0
GM22594
 
Resource Report
Resource Website 		RRID:CVCL_5R87 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM22594,
Wikidata:Q54852643		 CVCL_5R87 2026-02-07 08:10:38 0
GM22631
 
Resource Report
Resource Website 		Coriell Cat# GM22631, RRID:CVCL_1K44 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Male Coriell GM22631 Coriell:GM22631,
Wikidata:Q54852672		 CVCL_1K44 2026-02-07 08:10:39 0
GM22593
 
Resource Report
Resource Website 		Coriell Cat# GM22593, RRID:CVCL_5R86 Homo sapiens (Human) Autism spectrum disorder PMID:23495136
PMID:23665875 		Transformed cell line Female 801-009 LCL Coriell GM22593 Coriell:GM22593,
Wikidata:Q54852642		 CVCL_5R86 2026-02-07 08:10:43 0
GM22628
 
Resource Report
Resource Website 		Coriell Cat# GM22628, RRID:CVCL_1K41 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Male Coriell GM22628 Coriell:GM22628,
Wikidata:Q54852669		 CVCL_1K41 2026-02-07 08:10:39 0
GM22625
 
Resource Report
Resource Website 		Coriell Cat# GM22625, RRID:CVCL_1K38 Homo sapiens (Human) Potocki-Shaffer syndrome PMID:23665875 Transformed cell line Female Coriell GM22625 Coriell:GM22625,
Wikidata:Q54852666		 CVCL_1K38 2026-02-07 08:10:39 0

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