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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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GM04938
 
Resource Report
Resource Website 		RRID:CVCL_8A07 Homo sapiens (Human) Tourette syndrome Population: Caucasian. Transformed cell line Female CLO:CLO_0025578,
Coriell:GM04938,
Wikidata:Q54838775		 CVCL_8A07 2026-09-19 05:27:48 0
GM04887
 
Resource Report
Resource Website 		RRID:CVCL_V574 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. PMID:6230415 Finite cell line Female GM 4887 CLO:CLO_0025777,
Coriell:GM04887,
Wikidata:Q54838742		 CVCL_V574 2026-09-19 05:27:47 0
GM04937
 
Resource Report
Resource Website 		RRID:CVCL_8A06 Homo sapiens (Human) Tourette syndrome Population: Caucasian. Finite cell line Female CLO:CLO_0025577,
Coriell:GM04937,
Wikidata:Q54838774		 CVCL_8A06 2026-09-19 05:27:48 0
GM04849
 
Resource Report
Resource Website 		RRID:CVCL_1I57 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. Finite cell line Female CLO:CLO_0018176,
Coriell:GM04849,
Wikidata:Q54838718		 CVCL_1I57 2026-09-19 05:27:47 0
GM04921
 
Resource Report
Resource Website 		Coriell Cat# GM04921, RRID:CVCL_2T09 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;8)(4qter->4p15::8p22->8pter;8qter->8p22::4p15->4pter) (Coriell=GM04921)., Population: Caucasian. Finite cell line Female Coriell GM04921 CLO:CLO_0025602,
Coriell:GM04921,
Wikidata:Q54838762		 CVCL_2T09 2026-09-19 05:27:48 0
GM04862
 
Resource Report
Resource Website 		Coriell Cat# GM04862, RRID:CVCL_2T07 Homo sapiens (Human) Karyotypic information: 46,XX,t(7;21)(7pter->7q36::21q21->21qter;21pter->21q21::7q36->7qter) (Coriell=GM04862)., Population: Caucasian. Finite cell line Female Coriell GM04862 CLO:CLO_0025794,
Coriell:GM04862,
Wikidata:Q54838731		 CVCL_2T07 2026-09-19 05:27:47 0
GM04857
 
Resource Report
Resource Website 		RRID:CVCL_1I63 Homo sapiens (Human) Huntington's disease Part of: Venezuelan Huntington disease kindreds subcollection. PMID:25928884
PMID:30256717 		Finite cell line Female CLO:CLO_0018184,
Coriell:GM04857,
Wikidata:Q54838724		 CVCL_1I63 2026-09-19 05:27:47 0
GM04937
 
Resource Report
Resource Website 		Coriell Cat# GM04937, RRID:CVCL_8A06 Homo sapiens (Human) Tourette syndrome Population: Caucasian. Finite cell line Female Coriell GM04937 CLO:CLO_0025577,
Coriell:GM04937,
Wikidata:Q54838774		 CVCL_8A06 2026-09-19 05:27:48 0
GM04910
 
Resource Report
Resource Website 		RRID:CVCL_VH33 Homo sapiens (Human) Bannayan syndrome Population: Caucasian; French/German. Finite cell line Female CLO:CLO_0025589,
Coriell:GM04910,
Wikidata:Q54838755		 CVCL_VH33 2026-09-19 05:27:48 0
GM05050
 
Resource Report
Resource Website 		RRID:CVCL_HQ65 Homo sapiens (Human) Transformed cell line Female CLO:CLO_0025631,
Coriell:GM05050,
Wikidata:Q54838831		 CVCL_HQ65 2026-09-19 05:27:49 0
GM04960
 
Resource Report
Resource Website 		RRID:CVCL_AA44 Homo sapiens (Human) Familial dysautonomia Population: Caucasian. Transformed cell line Female CLO:CLO_0025580,
Coriell:GM04960,
Wikidata:Q54838787		 CVCL_AA44 2026-09-19 05:27:48 0
GM05042
 
Resource Report
Resource Website 		RRID:CVCL_AA48 Homo sapiens (Human) Familial dysautonomia Population: Jewish; Ashkenazi. Transformed cell line Female CLO:CLO_0025614,
Coriell:GM05042,
Wikidata:Q54838823		 CVCL_AA48 2026-09-19 05:27:49 0
GM05052
 
Resource Report
Resource Website 		RRID:CVCL_N036 Homo sapiens (Human) Population: African American., Part of: Human variation panel. Transformed cell line Female 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 2026-09-19 05:27:49 0
GM05011
 
Resource Report
Resource Website 		Coriell Cat# GM05011, RRID:CVCL_X135 Homo sapiens (Human) Population: Caucasian. PMID:6661932
PMID:23665875 		Transformed cell line Female GM-5011, GM 5011, GM05011A Coriell GM05011 CLO:CLO_0025669,
Coriell:GM05011,
Wikidata:Q54838810		 CVCL_X135 2026-09-19 05:27:49 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 2026-09-19 05:27:48 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 2026-09-19 05:27:49 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 2026-09-19 05:27:48 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 2026-09-19 05:27:48 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 2026-09-19 05:27:49 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 2026-09-19 05:27:48 0

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