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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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GM15864
 
Resource Report
Resource Website 		RRID:CVCL_AM74 Homo sapiens (Human) Ehlers-Danlos syndrome Population: Caucasian. Transformed cell line Female CLO:CLO_0018532,
Coriell:GM15864,
Wikidata:Q54848242		 CVCL_AM74 2026-08-15 04:32:33 0
GM15879
 
Resource Report
Resource Website 		RRID:CVCL_LH35 Homo sapiens (Human) Anhidrotic ectodermal dysplasia 1 Transformed cell line Female CLO:CLO_0018672,
Coriell:GM15879,
Wikidata:Q54848250		 CVCL_LH35 2026-08-15 04:32:33 0
GM15762
 
Resource Report
Resource Website 		RRID:CVCL_AT24 Homo sapiens (Human) Population: Caucasian; Icelandic., Part of: Human variation panel. Transformed cell line Female CLO:CLO_0027709,
Coriell:GM15762,
Wikidata:Q54848191		 CVCL_AT24 2026-08-15 04:32:32 0
GM15844
 
Resource Report
Resource Website 		RRID:CVCL_L024 Homo sapiens (Human) Parkinson disease 4, autosomal dominant Population: Caucasian. Transformed cell line Female CLO:CLO_0027793,
Coriell:GM15844,
Wikidata:Q54848227		 CVCL_L024 2026-08-15 04:32:32 0
GM15877
 
Resource Report
Resource Website 		RRID:CVCL_F508 Homo sapiens (Human) Xeroderma pigmentosum, complementation group D Characteristics: Transfection of wild type ERCC2 corrects the defects of this gene in the cell line., Population: Caucasian. PMID:8033104
PMID:18470933 		Transformed cell line Female D6BE-ER2-9, XP6BE-ER2-9, XP6BE ER2-9 CLO:CLO_0018646,
Coriell:GM15877,
Wikidata:Q54848249		 cvcl_f505 CVCL_F508 2026-08-15 04:32:33 0
GM15810
 
Resource Report
Resource Website 		RRID:CVCL_0Q33 Homo sapiens (Human) PMID:16809669 Transformed cell line Female CLO:CLO_0027747,
Coriell:GM15810,
GEO:GSM89126,
Wikidata:Q54848208		 CVCL_0Q33 2026-08-15 04:32:32 0
GM15762
 
Resource Report
Resource Website 		Coriell Cat# GM15762, RRID:CVCL_AT24 Homo sapiens (Human) Population: Caucasian; Icelandic., Part of: Human variation panel. Transformed cell line Female Coriell GM15762 CLO:CLO_0027709,
Coriell:GM15762,
Wikidata:Q54848191		 CVCL_AT24 2026-08-15 04:32:32 0
GM15763
 
Resource Report
Resource Website 		RRID:CVCL_AT25 Homo sapiens (Human) Population: Caucasian; Icelandic., Part of: Human variation panel. Transformed cell line Female CLO:CLO_0027707,
Coriell:GM15763,
Wikidata:Q54848192		 CVCL_AT25 2026-08-15 04:32:32 0
GM15822
 
Resource Report
Resource Website 		RRID:CVCL_0Q41 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0027763,
Coriell:GM15822,
Wikidata:Q54848221		 CVCL_0Q41 2026-08-15 04:32:32 0
GM16098
 
Resource Report
Resource Website
Possibly Discontinued 		RRID:CVCL_5Q62 Homo sapiens (Human) Nijmegen breakage syndrome PMID:23665875 Finite cell line Female Coriell:GM16098,
Wikidata:Q54848320		 CVCL_5Q62 2026-08-15 04:32:34 0
GM15891
 
Resource Report
Resource Website 		RRID:CVCL_N254 Homo sapiens (Human) Population: Caucasian; Iberian., Part of: Human variation panel. Transformed cell line Female GM17099 CLO:CLO_0014535,
CLO:CLO_0018630,
Coriell:GM15891,
Coriell:GM17099,
Wikidata:Q54848260		 CVCL_N254 2026-08-15 04:32:33 0
GM15904
 
Resource Report
Resource Website 		Coriell Cat# GM15904, RRID:CVCL_FW05 Homo sapiens (Human) Parkinson disease Transformed cell line Female Coriell GM15904 CLO:CLO_0018620,
BioSample:SAMN00804252,
Coriell:GM15904,
Wikidata:Q54848267		 CVCL_FW05 2026-08-15 04:32:33 0
GM15993
 
Resource Report
Resource Website 		Coriell Cat# GM15993, RRID:CVCL_2U46 Homo sapiens (Human) Transformed cell line Female Coriell GM15993 CLO:CLO_0018697,
Coriell:GM15993,
Wikidata:Q54848289		 CVCL_2U46 2026-08-15 04:32:34 0
GM15891
 
Resource Report
Resource Website 		Coriell Cat# GM15891, RRID:CVCL_N254 Homo sapiens (Human) Population: Caucasian; Iberian., Part of: Human variation panel. Transformed cell line Female GM17099 Coriell GM15891 CLO:CLO_0014535,
CLO:CLO_0018630,
Coriell:GM15891,
Coriell:GM17099,
Wikidata:Q54848260		 CVCL_N254 2026-08-15 04:32:33 0
GM16085
 
Resource Report
Resource Website 		RRID:CVCL_DA40 Homo sapiens (Human) Neuronal ceroid lipofuscinosis type 1 Transformed cell line Female CLO:CLO_0018781,
Coriell:GM16085,
Wikidata:Q54848315		 CVCL_DA40 2026-08-15 04:32:34 0
GM15913
 
Resource Report
Resource Website 		RRID:CVCL_5Q61 Homo sapiens (Human) Waardenburg syndrome type 4 Population: African American. PMID:23665875 Transformed cell line Female Coriell:GM15913,
Wikidata:Q54848276		 CVCL_5Q61 2026-08-15 04:32:33 0
GM15890
 
Resource Report
Resource Website 		Coriell Cat# GM17098, RRID:CVCL_N253 Homo sapiens (Human) Population: Caucasian; Iberian., Part of: Human variation panel. Transformed cell line Female GM17098 Coriell GM17098 CLO:CLO_0014533,
CLO:CLO_0018656,
Coriell:GM15890,
Coriell:GM17098,
Wikidata:Q54848259		 CVCL_N253 2026-08-15 04:32:33 0
GM15892
 
Resource Report
Resource Website 		Coriell Cat# GM17100, RRID:CVCL_N255 Homo sapiens (Human) Population: Caucasian; Iberian., Part of: Human variation panel. Transformed cell line Female GM17100 Coriell GM17100 CLO:CLO_0014893,
CLO:CLO_0018629,
Coriell:GM15892,
Coriell:GM17100,
Wikidata:Q54848261		 CVCL_N255 2026-08-15 04:32:33 0
GM15883
 
Resource Report
Resource Website 		RRID:CVCL_AT29 Homo sapiens (Human) Population: Caucasian; Basque., Part of: Human variation panel. Transformed cell line Female CLO:CLO_0018664,
Coriell:GM15883,
Wikidata:Q54848252		 CVCL_AT29 2026-08-15 04:32:33 0
GM15893
 
Resource Report
Resource Website 		Coriell Cat# GM15893, RRID:CVCL_FW02 Homo sapiens (Human) Parkinson disease Transformed cell line Female Coriell GM15893 CLO:CLO_0018628,
BioSample:SAMN00804244,
Coriell:GM15893,
Wikidata:Q54848263		 CVCL_FW02 2026-08-15 04:32:33 0

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