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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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236,573 Results - per page

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GM04952
 
Resource Report
Resource Website 		RRID:CVCL_GQ32 Homo sapiens (Human) Bipolar disorder Transformed cell line Male GM04952A CLO:CLO_0025587,
Coriell:GM04952,
Wikidata:Q54838783		 CVCL_GQ32 2026-08-08 05:00:21 0
GM04939
 
Resource Report
Resource Website 		RRID:CVCL_AB35 Homo sapiens (Human) Triploidy syndrome Karyotypic information: 69,XXX (Coriell=GM04939)., Population: Caucasian. Finite cell line Female CLO:CLO_0025569,
Coriell:GM04939,
Wikidata:Q54838776		 CVCL_AB35 2026-08-08 05:00:22 0
GM05058
 
Resource Report
Resource Website 		Coriell Cat# GM05058, RRID:CVCL_AK98 Homo sapiens (Human) Retinitis pigmentosa PMID:6726265 Transformed cell line Female RB 5058 Coriell GM05058 CLO:CLO_0025634,
Coriell:GM05058,
Wikidata:Q54838837		 CVCL_AK98 2026-08-08 05:00:22 0
GM04959
 
Resource Report
Resource Website 		RRID:CVCL_AA43 Homo sapiens (Human) Familial dysautonomia Population: Caucasian. Finite cell line Female CLO:CLO_0025586,
Coriell:GM04959,
Wikidata:Q54838786		 CVCL_AA43 2026-08-08 05:00:22 0
GM04981
 
Resource Report
Resource Website 		RRID:CVCL_8521 Homo sapiens (Human) Becker's muscular dystrophy Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:18691744
PMID:21354051
PMID:23665875 		Finite cell line Male CLO:CLO_0025653,
Coriell:GM04981,
Wikidata:Q54838791		 CVCL_8521 2026-08-08 05:00:21 0
GM04942
 
Resource Report
Resource Website 		Coriell Cat# GM04942, RRID:CVCL_GQ28 Homo sapiens (Human) Bipolar disorder Transformed cell line Female GM04942B Coriell GM04942 CLO:CLO_0025571,
Coriell:GM04942,
Wikidata:Q54838778		 CVCL_GQ28 2026-08-08 05:00:21 0
GM05060
 
Resource Report
Resource Website 		Coriell Cat# GM05060, RRID:CVCL_AL00 Homo sapiens (Human) Retinitis pigmentosa PMID:6726265 Transformed cell line Female RB 5060 Coriell GM05060 CLO:CLO_0025342,
Coriell:GM05060,
Wikidata:Q54838839		 CVCL_AL00 2026-08-08 05:00:23 0
GM05041
 
Resource Report
Resource Website 		RRID:CVCL_AA47 Homo sapiens (Human) Familial dysautonomia Population: Jewish; Ashkenazi. Transformed cell line Male GM05041A CLO:CLO_0025611,
Coriell:GM05041,
Wikidata:Q54838822		 CVCL_AA47 2026-08-08 05:00:23 0
GM04942
 
Resource Report
Resource Website 		RRID:CVCL_GQ28 Homo sapiens (Human) Bipolar disorder Transformed cell line Female GM04942B CLO:CLO_0025571,
Coriell:GM04942,
Wikidata:Q54838778		 CVCL_GQ28 2026-08-08 05:00:21 0
GM04948
 
Resource Report
Resource Website 		RRID:CVCL_9W98 Homo sapiens (Human) Finite cell line Male CLO:CLO_0025584,
Coriell:GM04948,
Wikidata:Q54838780		 CVCL_9W98 2026-08-08 05:00:21 0
GM05052
 
Resource Report
Resource Website 		Coriell Cat# GM17158, RRID:CVCL_N036 Homo sapiens (Human) Population: African American., Part of: Human variation panel. Transformed cell line Female GM17158 Coriell GM17158 CLO:CLO_0013965,
CLO:CLO_0025629,
Coriell:GM05052,
Coriell:GM17158,
GEO:GSM273425,
GEO:GSM569647,
GEO:GSM596223,
GEO:GSM597023,
GEO:GSM924668,
Wikidata:Q54838834		 CVCL_N036 2026-08-08 05:00:22 0
GM05048
 
Resource Report
Resource Website 		Coriell Cat# GM05048, RRID:CVCL_7416 Homo sapiens (Human) Transformed cell line Male Coriell GM05048 CLO:CLO_0025647,
Coriell:GM05048,
Wikidata:Q54838829		 CVCL_7416 2026-08-08 05:00:22 0
GM04952
 
Resource Report
Resource Website 		Coriell Cat# GM04952, RRID:CVCL_GQ32 Homo sapiens (Human) Bipolar disorder Transformed cell line Male GM04952A Coriell GM04952 CLO:CLO_0025587,
Coriell:GM04952,
Wikidata:Q54838783		 CVCL_GQ32 2026-08-08 05:00:22 0
GM05046
 
Resource Report
Resource Website 		RRID:CVCL_AA51 Homo sapiens (Human) Population: Jewish; Ashkenazi., Part of: Genetic Testing Reference Material (GeT-RM) samples. PMID:19815695 Transformed cell line Female GM05046A CLO:CLO_0025648,
Coriell:GM05046,
Wikidata:Q54838827		 CVCL_AA51 2026-08-08 05:00:23 0
GM05016
 
Resource Report
Resource Website 		RRID:CVCL_5N01 Homo sapiens (Human) Duchenne muscular dystrophy PMID:23665875 Transformed cell line Male CLO:CLO_0025677,
Coriell:GM05016,
Wikidata:Q54838812		 CVCL_5N01 2026-08-08 05:00:21 0
GM04965
 
Resource Report
Resource Website 		Coriell Cat# GM04965, RRID:CVCL_V479 Homo sapiens (Human) Down syndrome Population: Asian. PMID:6661932 Finite cell line Male GM 04965 Coriell GM04965 CLO:CLO_0025581,
Coriell:GM04965,
Wikidata:Q54838788		 CVCL_V479 2026-08-08 05:00:22 0
GM04986
 
Resource Report
Resource Website 		Coriell Cat# GM04986, RRID:CVCL_GQ36 Homo sapiens (Human) Bipolar disorder Population: Caucasian. Transformed cell line Male GM04986A Coriell GM04986 CLO:CLO_0025649,
Coriell:GM04986,
Wikidata:Q54838796		 CVCL_GQ36 2026-08-08 05:00:22 0
GM05081
 
Resource Report
Resource Website 		RRID:CVCL_U480 Homo sapiens (Human) Becker's muscular dystrophy Population: Caucasian. Finite cell line Male CLO:CLO_0025341,
Coriell:GM05081,
Wikidata:Q54838844		 CVCL_U480 2026-08-08 05:00:23 0
GM05010
 
Resource Report
Resource Website 		Coriell Cat# GM05010, RRID:CVCL_X134 Homo sapiens (Human) Karyotypic information: 46,X,t(X;8;2)(Xpter->Xq21.2::2q14.2->2qter;8qter->8p11.1::Xq21.2->Xqter;2pter->2q14.2::8p11.1->8pter) (Coriell=GM05010)., Population: Caucasian. PMID:6661932 Finite cell line Female GM-5010, GM 5010 Coriell GM05010 CLO:CLO_0025670,
Coriell:GM05010,
Wikidata:Q54838809		 CVCL_X134 2026-08-08 05:00:21 0
GM05007
 
Resource Report
Resource Website 		RRID:CVCL_GS67 Homo sapiens (Human) Erythropoietic protoporphyria Population: Caucasian. PMID:1376018 Finite cell line Male GM05007A CLO:CLO_0025673,
Coriell:GM05007,
Wikidata:Q54838806		 CVCL_GS67 2026-08-08 05:00:21 0

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