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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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  • References:pmid:23665875 (facet)

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GM23830
 
Resource Report
Resource Website 		RRID:CVCL_5T21 Homo sapiens (Human) Isodicentric chromosome PMID:23665875 Transformed cell line Female Coriell:GM23830,
Wikidata:Q54853358		 CVCL_5T21 2026-09-05 10:59:41 0
GM23899
 
Resource Report
Resource Website 		RRID:CVCL_U555 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell:GM23899,
Wikidata:Q54853428		 CVCL_U555 2026-09-05 10:59:42 0
GM23854
 
Resource Report
Resource Website 		Coriell Cat# GM23854, RRID:CVCL_5T23 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM23854 Coriell:GM23854,
Wikidata:Q54853378		 CVCL_5T23 2026-09-05 10:59:41 0
GM23857
 
Resource Report
Resource Website 		RRID:CVCL_U552 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Male Coriell:GM23857,
Wikidata:Q54853380		 CVCL_U552 2026-09-05 10:59:41 0
GM23854
 
Resource Report
Resource Website 		RRID:CVCL_5T23 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM23854,
Wikidata:Q54853378		 CVCL_5T23 2026-09-05 10:59:41 0
GM23832
 
Resource Report
Resource Website 		Coriell Cat# GM23832, RRID:CVCL_U550 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell GM23832 Coriell:GM23832,
Wikidata:Q54853361		 CVCL_U550 2026-09-05 10:59:41 0
GM23873
 
Resource Report
Resource Website 		Coriell Cat# GM23873, RRID:CVCL_5T25 Homo sapiens (Human) PMID:23665875
PMID:26621101
PMID:29474986 		Transformed cell line Female Coriell GM23873 Coriell:GM23873,
Wikidata:Q54853409		 CVCL_5T25 2026-09-05 10:59:42 0
GM23862
 
Resource Report
Resource Website 		RRID:CVCL_U553 Homo sapiens (Human) Prader-Willi syndrome PMID:23665875 Transformed cell line Female Coriell:GM23862,
Wikidata:Q54853384		 CVCL_U553 2026-09-05 10:59:41 0
GM23922
 
Resource Report
Resource Website 		RRID:CVCL_5T38 Homo sapiens (Human) Hyperglycerolemia PMID:23665875 Transformed cell line Male Coriell:GM23922,
Wikidata:Q54853442		 CVCL_5T38 2026-09-05 10:59:42 0
GM23905
 
Resource Report
Resource Website 		Coriell Cat# GM23905, RRID:CVCL_5T32 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM23905 Coriell:GM23905,
Wikidata:Q54853431		 CVCL_5T32 2026-09-05 10:59:42 0
GM23906
 
Resource Report
Resource Website
Possibly Discontinued 		RRID:CVCL_5T33 Homo sapiens (Human) Hyperglycerolemia PMID:23665875 Transformed cell line Male Coriell:GM23906,
Wikidata:Q54853432		 CVCL_5T33 2026-09-05 10:59:42 0
GM23900
 
Resource Report
Resource Website 		Coriell Cat# GM23900, RRID:CVCL_5T30 Homo sapiens (Human) Turner syndrome PMID:23665875 Transformed cell line Female Coriell GM23900 Coriell:GM23900,
Wikidata:Q54853429		 CVCL_5T30 2026-09-05 10:59:42 0
GM23905
 
Resource Report
Resource Website 		RRID:CVCL_5T32 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM23905,
Wikidata:Q54853431		 CVCL_5T32 2026-09-05 10:59:42 0
GM23908
 
Resource Report
Resource Website 		RRID:CVCL_5T35 Homo sapiens (Human) Congenital adrenal gland hypoplasia PMID:23665875 Transformed cell line Male Coriell:GM23908,
Wikidata:Q54853434		 CVCL_5T35 2026-09-05 10:59:42 0
GM23904
 
Resource Report
Resource Website 		RRID:CVCL_5T31 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell:GM23904,
Wikidata:Q54853430		 CVCL_5T31 2026-09-05 10:59:42 0
GM23922
 
Resource Report
Resource Website 		Coriell Cat# GM23922, RRID:CVCL_5T38 Homo sapiens (Human) Hyperglycerolemia PMID:23665875 Transformed cell line Male Coriell GM23922 Coriell:GM23922,
Wikidata:Q54853442		 CVCL_5T38 2026-09-05 10:59:42 0
GM23904
 
Resource Report
Resource Website 		Coriell Cat# GM23904, RRID:CVCL_5T31 Homo sapiens (Human) PMID:23665875 Transformed cell line Male Coriell GM23904 Coriell:GM23904,
Wikidata:Q54853430		 CVCL_5T31 2026-09-05 10:59:42 0
GM50142
 
Resource Report
Resource Website 		RRID:CVCL_5T49 Homo sapiens (Human) PMID:23665875 Transformed cell line Male JL263 CLO:CLO_0014676,
Coriell:GM50142,
Wikidata:Q54854217		 CVCL_5T49 2026-09-05 11:00:15 0
GM50168
 
Resource Report
Resource Website 		RRID:CVCL_5L31 Homo sapiens (Human) Deletion 18q syndrome PMID:23665875 Transformed cell line Male JL339 CLO:CLO_0015018,
Coriell:GM50168,
Wikidata:Q54854241		 CVCL_5L31 2026-09-05 11:00:16 0
GM50152
 
Resource Report
Resource Website 		Coriell Cat# GM50152, RRID:CVCL_5L26 Homo sapiens (Human) Deletion 18p syndrome PMID:23665875 Transformed cell line Female JL280 Coriell GM50152 CLO:CLO_0014709,
Coriell:GM50152,
Wikidata:Q54854225		 CVCL_5L26 2026-09-05 11:00:15 0

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