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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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GM16968
 
Resource Report
Resource Website 		Coriell Cat# GM16968, RRID:CVCL_4D34 Homo sapiens (Human) Population: Caucasian; Amish. Finite cell line Female Coriell GM16968 CLO:CLO_0018085,
Coriell:GM16968,
Wikidata:Q54848823		 CVCL_4D34 2026-08-15 04:32:44 0
GM16866
 
Resource Report
Resource Website
1+ mentions 		RRID:CVCL_4F75 Homo sapiens (Human) Peroxisome biogenesis disorder 7A Population: Caucasian. PMID:12851857
PMID:16257970 		Finite cell line Female CLO:CLO_0018133,
Coriell:GM16866,
Wikidata:Q54848793		 CVCL_4F75 2026-08-15 04:32:43 1
GM16772
 
Resource Report
Resource Website 		RRID:CVCL_AB22 Homo sapiens (Human) Familial dysautonomia Donor information: Established from monozygotic twin of GM16771 (Cellosaurus=CVCL_AB21)., Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0018441,
Coriell:GM16772,
Wikidata:Q54848732		 CVCL_AB22 2026-08-15 04:32:43 0
GM16966
 
Resource Report
Resource Website 		RRID:CVCL_4D32 Homo sapiens (Human) Population: Caucasian; Amish. Finite cell line Female CLO:CLO_0018082,
Coriell:GM16966,
Wikidata:Q54848821		 CVCL_4D32 2026-08-15 04:32:44 0
GM16799
 
Resource Report
Resource Website 		RRID:CVCL_1F67 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female CLO:CLO_0018398,
Coriell:GM16799,
Wikidata:Q54848749		 CVCL_1F67 2026-08-15 04:32:43 0
GM16787
 
Resource Report
Resource Website 		Coriell Cat# GM16787, RRID:CVCL_CZ71 Homo sapiens (Human) Population: Caucasian; Sardinian. Transformed cell line Female Coriell GM16787 CLO:CLO_0018383,
Coriell:GM16787,
Wikidata:Q54848740		 CVCL_CZ71 2026-08-15 04:32:43 0
GM16965
 
Resource Report
Resource Website 		RRID:CVCL_4D31 Homo sapiens (Human) Population: Caucasian; Amish. Transformed cell line Female CLO:CLO_0018083,
Coriell:GM16965,
Wikidata:Q54848820		 CVCL_4D31 2026-08-15 04:32:44 0
GM16800
 
Resource Report
Resource Website 		Coriell Cat# GM16800, RRID:CVCL_1F68 Homo sapiens (Human) Population: Caucasian. Finite cell line Female Coriell GM16800 CLO:CLO_0018395,
Coriell:GM16800,
Wikidata:Q54848750		 CVCL_1F68 2026-08-15 04:32:43 0
GM16865
 
Resource Report
Resource Website 		RRID:CVCL_9Z52 Homo sapiens (Human) Peroxisome biogenesis disorder 7B Population: Caucasian. PMID:12851857 Finite cell line Female CLO:CLO_0018130,
Coriell:GM16865,
Wikidata:Q54848792		 CVCL_9Z52 2026-08-15 04:32:43 0
GM16754
 
Resource Report
Resource Website 		Coriell Cat# GM16754, RRID:CVCL_AK43 Homo sapiens (Human) Fanconi anemia, complementation group C Finite cell line Female PD331.F, PD331.f, PD331 Coriell GM16754 CLO:CLO_0018428,
Coriell:GM16754,
Wikidata:Q54848723		 CVCL_AK43 2026-08-15 04:32:42 0
GM16799
 
Resource Report
Resource Website 		Coriell Cat# GM16799, RRID:CVCL_1F67 Homo sapiens (Human) Population: Caucasian. Transformed cell line Female Coriell GM16799 CLO:CLO_0018398,
Coriell:GM16799,
Wikidata:Q54848749		 CVCL_1F67 2026-08-15 04:32:43 0
GM16966
 
Resource Report
Resource Website 		Coriell Cat# GM16966, RRID:CVCL_4D32 Homo sapiens (Human) Population: Caucasian; Amish. Finite cell line Female Coriell GM16966 CLO:CLO_0018082,
Coriell:GM16966,
Wikidata:Q54848821		 CVCL_4D32 2026-08-15 04:32:44 0
GM16808
 
Resource Report
Resource Website 		RRID:CVCL_5Q79 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell:GM16808,
Wikidata:Q54848755		 CVCL_5Q79 2026-08-15 04:32:43 0
GM16774
 
Resource Report
Resource Website 		Coriell Cat# GM18098, RRID:CVCL_N268 Homo sapiens (Human) Population: Caucasian; French Canadian., Part of: Human variation panel. Transformed cell line Female GM18098 Coriell GM18098 CLO:CLO_0015751,
CLO:CLO_0018442,
Coriell:GM16774,
Coriell:GM18098,
Wikidata:Q54848733		 CVCL_N268 2026-08-15 04:32:43 0
GM16768
 
Resource Report
Resource Website 		RRID:CVCL_AB18 Homo sapiens (Human) Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0018432,
Coriell:GM16768,
Wikidata:Q54848728		 CVCL_AB18 2026-08-15 04:32:42 0
GM16798
 
Resource Report
Resource Website
1+ mentions 		RRID:CVCL_U754 Homo sapiens (Human) Friedreich ataxia Transformed cell line Female CLO:CLO_0018397,
Coriell:GM16798,
Wikidata:Q54848747		 CVCL_U754 2026-08-15 04:32:43 1
GM16810
 
Resource Report
Resource Website 		Coriell Cat# GM16810, RRID:CVCL_5Q81 Homo sapiens (Human) PMID:23665875 Transformed cell line Female Coriell GM16810 Coriell:GM16810,
Wikidata:Q54848757		 CVCL_5Q81 2026-08-15 04:32:43 0
GM16967
 
Resource Report
Resource Website 		Coriell Cat# GM16967, RRID:CVCL_4D33 Homo sapiens (Human) Population: Caucasian; Amish. Transformed cell line Female Coriell GM16967 CLO:CLO_0018087,
Coriell:GM16967,
Wikidata:Q54848822		 CVCL_4D33 2026-08-15 04:32:44 0
GM16771
 
Resource Report
Resource Website 		RRID:CVCL_AB21 Homo sapiens (Human) Familial dysautonomia Donor information: Established from monozygotic twin of GM16772 (Cellosaurus=CVCL_AB22)., Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0018440,
Coriell:GM16771,
Wikidata:Q54848731		 CVCL_AB21 2026-08-15 04:32:43 0
GM16923
 
Resource Report
Resource Website 		RRID:CVCL_4D26 Homo sapiens (Human) Osteogenesis imperfecta type IV Population: Caucasian; Amish. Finite cell line Female CLO:CLO_0018104,
Coriell:GM16923,
Wikidata:Q54848805		 CVCL_4D26 2026-08-15 04:32:44 0

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