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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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GM04723
 
Resource Report
Resource Website 		Coriell Cat# GM04723, RRID:CVCL_Y871 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female Coriell GM04723 CLO:CLO_0019072,
Coriell:GM04723,
Wikidata:Q54838655		 CVCL_Y871 2026-08-08 05:00:17 0
GM04734
 
Resource Report
Resource Website 		RRID:CVCL_1I28 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04734A CLO:CLO_0019069,
Coriell:GM04734,
Wikidata:Q54838661		 CVCL_1I28 2026-08-08 05:00:18 0
GM04610
 
Resource Report
Resource Website 		Coriell Cat# GM04610, RRID:CVCL_X309 Homo sapiens (Human) Trisomy 8 Karyotypic information: 47,XX,+8 [75]; 46,XX,+8,dic(14;21)(14qter->14p13::21p13->21qter) [25] (Coriell=GM04610). PMID:6661932 Finite cell line Female GM 4610 Coriell GM04610 CLO:CLO_0018902,
Coriell:GM04610,
Wikidata:Q54838597		 CVCL_X309 2026-08-08 05:00:16 0
GM04718
 
Resource Report
Resource Website 		RRID:CVCL_V569 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04718A CLO:CLO_0019022,
Coriell:GM04718,
Wikidata:Q54838650		 CVCL_V569 2026-08-08 05:00:18 0
GM04608
 
Resource Report
Resource Website 		Coriell Cat# GM04608, RRID:CVCL_Y797 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian. Finite cell line Female Coriell GM04608 CLO:CLO_0018912,
Coriell:GM04608,
Wikidata:Q54838596		 CVCL_Y797 2026-08-08 05:00:17 0
GM04708
 
Resource Report
Resource Website 		Coriell Cat# GM04708, RRID:CVCL_1I26 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04708A Coriell GM04708 CLO:CLO_0019025,
Coriell:GM04708,
Wikidata:Q54838642		 CVCL_1I26 2026-08-08 05:00:18 0
GM04720
 
Resource Report
Resource Website 		Coriell Cat# GM04720, RRID:CVCL_0I33 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04720A Coriell GM04720 CLO:CLO_0019077,
Coriell:GM04720,
Wikidata:Q54838652		 CVCL_0I33 2026-08-08 05:00:17 0
GM04681
 
Resource Report
Resource Website 		Coriell Cat# GM04681, RRID:CVCL_AT05 Homo sapiens (Human) Multiple sulfatase deficiency disease Population: Caucasian. PMID:6132606 Finite cell line Male GM 4681 Coriell GM04681 CLO:CLO_0019037,
Coriell:GM04681,
Wikidata:Q54838627		 CVCL_AT05 2026-08-08 05:00:17 0
GM04709
 
Resource Report
Resource Website 		Coriell Cat# GM04709, RRID:CVCL_Y863 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female Coriell GM04709 CLO:CLO_0019026,
Coriell:GM04709,
Wikidata:Q54838643		 CVCL_Y863 2026-08-08 05:00:17 0
GM04674
 
Resource Report
Resource Website 		RRID:CVCL_9R22 Homo sapiens (Human) Population: Caucasian. PMID:19127062 Transformed cell line Female GM04674A CLO:CLO_0019012,
Coriell:GM04674,
Wikidata:Q54838626		 CVCL_9R22 2026-08-08 05:00:17 0
GM04715
 
Resource Report
Resource Website 		Coriell Cat# GM04715, RRID:CVCL_Y865 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male Coriell GM04715 CLO:CLO_0019019,
Coriell:GM04715,
Wikidata:Q54838646		 CVCL_Y865 2026-08-08 05:00:17 0
GM04688
 
Resource Report
Resource Website 		RRID:CVCL_Y862 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female GM04688A CLO:CLO_0019035,
Coriell:GM04688,
Wikidata:Q54838630		 CVCL_Y862 2026-08-08 05:00:16 0
GM04716
 
Resource Report
Resource Website 		RRID:CVCL_Y866 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Male GM04716A CLO:CLO_0019020,
Coriell:GM04716,
Wikidata:Q54838647		 CVCL_Y866 2026-08-08 05:00:18 0
GM04726
 
Resource Report
Resource Website 		RRID:CVCL_HJ75 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female Coriell:GM04726,
Wikidata:Q54838657		 CVCL_HJ75 2026-08-08 05:00:17 0
GM04726
 
Resource Report
Resource Website 		Coriell Cat# GM04726, RRID:CVCL_HJ75 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Transformed cell line Female Coriell GM04726 Coriell:GM04726,
Wikidata:Q54838657		 CVCL_HJ75 2026-08-08 05:00:17 0
GM04617
 
Resource Report
Resource Website 		Coriell Cat# GM04617, RRID:CVCL_V476 Homo sapiens (Human) Down syndrome Karyotypic information: 47,XX,+21[25].arr(21)x3 (Coriell=GM04617)., Population: Puerto Rican. PMID:6661932 Finite cell line Female GM 4617 Coriell GM04617 CLO:CLO_0018953,
Coriell:GM04617,
Wikidata:Q54838602		 CVCL_V476 2026-08-08 05:00:16 0
GM04717
 
Resource Report
Resource Website 		RRID:CVCL_V568 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female CLO:CLO_0019021,
Coriell:GM04717,
Wikidata:Q54838649		 CVCL_V568 2026-08-08 05:00:17 0
GM04711
 
Resource Report
Resource Website 		Coriell Cat# GM04711, RRID:CVCL_1I27 Homo sapiens (Human) Part of: Venezuelan Huntington disease kindreds subcollection. PMID:6230415 Finite cell line Male GM 4711 Coriell GM04711 CLO:CLO_0019018,
Coriell:GM04711,
Wikidata:Q54838645		 CVCL_1I27 2026-08-08 05:00:18 0
GM04693
 
Resource Report
Resource Website 		RRID:CVCL_Y878 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Male CLO:CLO_0019032,
Coriell:GM04693,
Wikidata:Q54838635		 CVCL_Y878 2026-08-08 05:00:18 0
GM04648
 
Resource Report
Resource Website 		RRID:CVCL_AW56 Homo sapiens (Human) Dystrophia myotonica 1 Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:23680132
PMID:32656337 		Transformed cell line Male CLO:CLO_0018967,
Coriell:GM04648,
Wikidata:Q54838619		 CVCL_AW56 2026-08-08 05:00:16 0

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